[{"data":1,"prerenderedAt":364},["ShallowReactive",2],{"2j58h0FQmBDSvyYTJ3RxY92GEKkdm2jz3PjAu7rzl8Y":3},{"data":4,"meta":360},[5],{"id":6,"documentId":7,"Name":8,"CompanyID":9,"Address":10,"RepresentativeName":11,"createdAt":12,"updatedAt":13,"publishedAt":14,"Foods":15},76493,"xxrd8juhneyxf2u9wbmn70zd","株式会社ＦＲＡＣＯＲＡ（旧社名：株式会社協和）","6013101003286","東京都福生市東町1番地1　主たる事務所所在地　〒160-0023　東京都新宿区西新宿1丁目22番2号　新宿サンエービル9F（パッケージには主たる事務所所在地を記載）","堀内　泰司","2025-05-22T13:27:41.294Z","2026-09-28T03:52:14.080Z","2026-09-28T03:52:14.085Z",[16,72,87,101,113,127,139,151,164,178,191,203,215,229,262,276,288,299,329],{"id":17,"documentId":18,"Name":19,"createdAt":20,"updatedAt":21,"publishedAt":22,"FID":23,"ModifyDate":24,"RepealDate":25,"SortNo":26,"RegistDate":27,"Class":28,"ComponentTxt":29,"FunctionFull":30,"SaleStatus":31,"Intake":32,"CategoryName":33,"Extract":34,"ConsumerContact":35,"Website":36,"ResponsibleBureau":37,"Tel":38,"TargetAudience":39,"SalesDate":40,"ModifyHistory20250331":41,"ModifyHistory20250401":42,"ReNotification":34,"IdentityReason":43,"Retraction":34,"RetractionTxt":43,"SelfInspection":44,"SelfInspectionChk1":45,"SelfInspectionChk2":45,"SelfInspectionChk3":45,"ExistingFID":43,"SelfInspectionChk4":45,"IntakeAmount":46,"PrecautionsTake":47,"HowToTake":46,"SafetySelf":48,"EatingResults":49,"FldWebsite":50,"OtherReasons":43,"NonEatingResults":34,"PublicDB2":43,"SafetyEvaluation2":43,"PrimaryInformation3":43,"SafetyEvaluation3":43,"PublicDB4":43,"SafetyEvaluation4":43,"PrimaryInformation5":49,"SafetyEvaluation5":51,"SafetyTest67":43,"ReferenceDB8":52,"Interaction1":43,"ReferenceDB9":43,"Interaction2":53,"ManufacturingSite1":53,"ManufacturingSite2":54,"ManufacturingSite3":55,"ManufacturingSite4":56,"ManufacturingSite5":57,"Location1":58,"Location2":59,"Location3":60,"Location4":61,"Location5":62,"SntermediateProducts1":45,"SntermediateProducts2":34,"SntermediateProducts3":34,"SntermediateProducts4":34,"SntermediateProducts5":34,"FinalProduct1":34,"FinalProduct2":45,"FinalProduct3":45,"FinalProduct4":45,"FinalProduct5":45,"ManufacturingStandards1":45,"ManufacturingStandards2":45,"ManufacturingStandards3":45,"ManufacturingStandards4":45,"ManufacturingStandards5":45,"FunctionSelf":63,"ManufacturingAddress":43,"ManufacturingInfo":64,"RawMaterials":65,"IndicatorComponent":43,"HealthDamage":66,"TelNo":35,"Email":43,"OtherContact":67,"AvailableHours":68,"AcademicConsensus":34,"Identity":34,"HumanTesting":34,"CITNo":43,"PeerReview":34,"TabletPositive":45,"PeerReviewNot":45,"HowToTakeB":45,"HowToSave":69,"SaveInfo1":70,"SaveInfo2":43,"OverdoseInfo":71,"SRproduct":34,"SRcomponent":45,"EatingResultsFinal":45,"EatingResultsSimilar":34,"Equivalence2":34,"Equivalence3":34,"Equivalence4":34,"Equivalence5":45,"PRISMA":43,"IngredientList":25},86729,"z8p8w1vn457r1nojlfnm5kta","フラコラ　ヒアルロン酸","2025-05-22T13:45:39.305Z","2026-09-28T03:09:05.408Z","2026-09-28T03:09:05.417Z","A158","2026-07-01",null,10158,"2015-10-08","加工食品(錠剤、カプセル剤等)","ヒアルロン酸Na","本品はヒアルロン酸Na120mgを含みます。ヒアルロン酸Naは肌の潤いを正常に保ち、乾燥を緩和する機能があることが報告されています。","販売中","120mg","ヒアルロン酸含有食品",false,"0120-57-2020","http://www.fracora.com/","研究開発部","03-5326-8001","肌の潤いを正常にしたい方、肌の乾燥が気になる方","2016-01-29","（2024年12月26日）様式Ⅳの修正","（2026.07.01）様式I 届出情報、届出書作成に当たっての確認事項、届出後の届出項目、様式III 錠剤、カプセル剤等食品の場合、【上記枠に記入しきれない場合、その他加工食品・生鮮食品の場合】、様式VI 表示及び情報開示の在り方に係る事項","","2026/3",true,"1日1粒を目安に、水またはぬるま湯とともにお召し上がりください。","＊本品は、大量摂取により疾病が治癒したり、より健康が増進するものではありません。１日の摂取目安量を守ってください。＊開封後はお早めにお召し上がりください。＊乳幼児の手の届かないところに保管してください。＊天然物由来原料を含むため、色調等に若干のバラツキがある場合もありますが、品質には問題ありません。＊食物アレルギーのある方は、原材料名をご参照の上お召し上がりください。","本品の機能性関与成分であるヒアルロン酸Naは、既存添加物「ヒアルロン酸」として食品の製造に使用されています。 ヒアルロン酸は、健康食品をはじめとする加工食品に使用されており、国内をはじめとして、韓国やアメリカ、カナダ等でも販売されています。 株式会社FRACORAでは、ヒアルロン酸を1日当たり120mg摂取できるソフトカプセル形態の栄養補助食品を2012年より全国で販売しており、これまでに累計24万袋以上販売しております。 また、原料供給元であるキユーピー株式会社では、ヒアルロン酸を1日当たり240mg摂取できるソフトカプセル形態の栄養補助食品を2002年より全国で販売しており、これまでに累計60万袋以上販売しております。 どちらもヒアルロン酸に起因する健康被害の報告はなく、また、「当該食品と類似する食品」の3要件を満たす食品です。 以上のような状況から本品に含まれるヒアルロン酸には十分な食経験があり、本品の１日摂取目安量を摂取した場合、人の健康を害する恐れはないと判断します。","あり","https://www.fld.caa.go.jp/caaks/s/cssc01/fwccd01?c__id=a09F900004sk8TeIAI","評価が十分","城西大学薬学部 食品‐医薬品相互作用データベース Ver.10.0","三生医薬株式会社　 南陵工場","三生医薬株式会社　 依田橋工場","三生医薬株式会社　 依田橋第二工場","三生医薬株式会社　 阿幸地工場","三生医薬株式会社　 富士根工場","静岡県富士宮市南陵12","静岡県富士市今泉花の木643-2","静岡県富士市今泉字三条319-1","静岡県富士宮市阿幸地町334","静岡県富士宮市小泉1661-1","標題「ヒアルロン酸Na経口摂取による肌の乾燥緩和機能について」  目的： 本研究レビューは、乾燥肌に悩む健常者がヒアルロン酸もしくはヒアルロン酸Naを経口摂取することにより、プラセボの経口摂取と比較して角層水分量が有意に高値を示すか検証することを目的として行いました。  背景： ヒアルロン酸は、皮膚，関節液など生体内のあらゆる結合組織，器官に存在しています。中でも皮膚には体内で最も多くのヒアルロン酸が存在しており、その量は全身に含まれる量の50％を占めると報告されています1)。体内においては、ヒアルロン酸Naとヒアルロン酸は共に溶解し、同様の働きをします。 一方で、ヒアルロン酸Naを経口摂取した機能性について個々の研究は複数実施されているものの、研究全体をまとめたレビューはありません。  レビュー対象とした研究の特性： 　英語文献検索サイトと日本語文献検索サイトおよび複数の学会誌のハンドサーチにより、2015年9月7日にキユーピー株式会社社員2名で検索し、アトピー性皮膚炎などの皮膚疾患のない、乾燥肌に悩む健常者がヒアルロン酸もしくはヒアルロン酸Naを経口摂取することによりプラセボに比べて、角質水分量が有意に高値を示すかを検証した臨床研究を選抜しました。なお、本研究レビューの採用文献4報のうち1報2）において、対象者は19～70歳の健常な男女でした。これに関して、厚生労働省による「日本人の食事摂取基準（2015年版）策定検討会報告書献3）」では、栄養摂取に関する年齢区分の設定を「18歳以上を成人」としています。そのため、18歳以上の未成年を含む論文も成人データとして扱うことは問題ないと考えました。  主な結果 文献検索により4報の文献2,4‐6）が抽出されました。4報の採用文献からエビデンス総体として120mgのヒアルロン酸Naを経口摂取することにより、プラセボの経口摂取と比較して有意に角層水分量が高値を示すことが検証されました。ヒアルロン酸Na摂取に起因する有害事象はありませんでした。  科学的根拠（エビデンス）の質 評価した文献の研究デザインは全て信頼性の高い試験系である無作為化コントロール比較試験であり、バイアスリスクの評価は低～中程度であったため、エビデンスの質は機能性の評価に値すると考えます。 研究レビューについては、本レビューで採用した研究データ以外にも、未発表の研究データが存在する可能性は否定できません。 研究論文の収集は、主要な医療分野のデータベースを使用して検索をしているものの、効果がないとする研究結果については論文として発表されていない可能性も考えられます。 研究間の結果の違いや各研究のデータのバラつきの評価において、本研究レビューは定性的レビューであるため、定量的な評価ができませんでした。そのため、独自の方法で評価を実施しました。 実施者であるキユーピー株式会社は本届出商品の機能性関与成分であるヒアルロン酸Naの原料メーカーであり、採用論文4報のうち3報はキユーピー株式会社の社員が著者であるが、研究レビューについては著者を除いた社員で公正に実施され、エビデンスと本届出商品に表示しようとする機能性に齟齬はないと考えられます。  参考文献 1）Laurent TC et al., Hyaluronan. FASEB J, 1992, 6:2397-2402. 2）佐藤稔秀ら, 乾燥肌におけるヒアルロン酸含有食品の経口摂取による臨床効果. Aesthetic Dermatology, 2002, 12:109-120. 3）厚生労働省，「日本人の食事摂取基準（2015年版）策定検討会報告書」 4）佐藤稔秀ら, 乾燥肌の皮膚水分値に対するヒアルロン酸含有食品の臨床効果. Aesthetic Dermatology, 2007, 17:33-39. 5）Kawada C et al., Ingestion of hyaluronans (molecular weights 800 k and 300 k) improves dry skin conditions: a randomized, double blind, controlled study. 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ビス－３－ヒドロキシ－３－メチルブチレートモノハイドレート（HMBカルシウム）には加齢による筋肉の減少を軽減し、日常生活をスムーズに行うために必要な筋肉量や筋力の維持をサポートする機能があることが報告されています。",{"id":230,"documentId":231,"Name":232,"createdAt":233,"updatedAt":234,"publishedAt":235,"FID":236,"ModifyDate":237,"RepealDate":238,"SortNo":239,"RegistDate":240,"Class":28,"ComponentTxt":241,"FunctionFull":242,"SaleStatus":86,"Intake":243,"CategoryName":244,"Extract":34,"ConsumerContact":35,"Website":245,"ResponsibleBureau":37,"Tel":38,"TargetAudience":246,"SalesDate":247,"ModifyHistory20250331":41,"ModifyHistory20250401":43,"ReNotification":34,"IdentityReason":43,"Retraction":45,"RetractionTxt":248,"SelfInspection":43,"SelfInspectionChk1":34,"SelfInspectionChk2":34,"SelfInspectionChk3":34,"ExistingFID":43,"SelfInspectionChk4":34,"IntakeAmount":249,"PrecautionsTake":250,"HowToTake":251,"SafetySelf":252,"EatingResults":49,"FldWebsite":253,"OtherReasons":43,"NonEatingResults":34,"PublicDB2":43,"SafetyEvaluation2":43,"PrimaryInformation3":43,"SafetyEvaluation3":43,"PublicDB4":43,"SafetyEvaluation4":43,"PrimaryInformation5":49,"SafetyEvaluation5":43,"SafetyTest67":43,"ReferenceDB8":254,"Interaction1":43,"ReferenceDB9":43,"Interaction2":43,"ManufacturingSite1":43,"ManufacturingSite2":43,"ManufacturingSite3":43,"ManufacturingSite4":43,"ManufacturingSite5":43,"Location1":43,"Location2":43,"Location3":43,"Location4":43,"Location5":43,"SntermediateProducts1":34,"SntermediateProducts2":34,"SntermediateProducts3":34,"SntermediateProducts4":34,"SntermediateProducts5":34,"FinalProduct1":34,"FinalProduct2":34,"FinalProduct3":34,"FinalProduct4":34,"FinalProduct5":34,"ManufacturingStandards1":34,"ManufacturingStandards2":34,"ManufacturingStandards3":34,"ManufacturingStandards4":34,"ManufacturingStandards5":34,"FunctionSelf":255,"ManufacturingAddress":256,"ManufacturingInfo":257,"RawMaterials":258,"IndicatorComponent":43,"HealthDamage":66,"TelNo":35,"Email":43,"OtherContact":259,"AvailableHours":260,"AcademicConsensus":34,"Identity":34,"HumanTesting":34,"CITNo":43,"PeerReview":34,"TabletPositive":45,"PeerReviewNot":45,"HowToTakeB":34,"HowToSave":69,"SaveInfo1":70,"SaveInfo2":43,"OverdoseInfo":261,"SRproduct":34,"SRcomponent":45,"EatingResultsFinal":34,"EatingResultsSimilar":45,"Equivalence2":34,"Equivalence3":34,"Equivalence4":34,"Equivalence5":34,"PRISMA":43,"IngredientList":25},89120,"qf27wbooidhqdkrxvagxmxht","大人の１粒習慣","2025-05-22T13:53:02.157Z","2026-09-28T03:27:52.965Z","2026-09-28T03:27:52.976Z","E478","2025-12-16","2026-03-26",50478,"2019-10-16","サラシア由来サラシノール","本品にはサラシア由来サラシノールが含まれます。サラシア由来サラシノールには食事から摂取した糖の吸収をおだやかにし、食後の血糖値の上昇をゆるやかにする機能があることが報告されています。","0.4㎎","サラシアエキス含有食品","http://www.fracora.com","健常成人（食事の糖質が気になる方、血糖値の上昇が気になる方）","2019-12-25","終売したため","２粒","●糖尿病の薬を服用されている方は、摂取前に医師、薬剤師に相談してください。 ●本品は、多量摂取により疾病が治癒したり、より健康が増進するものではありません。　 　１日の摂取目安量を守ってください。 ●原材料名をご参照の上、食物アレルギーのある方は摂取しないでください。 ●乳幼児の手の届かないところに保管してください。 ●色調等に若干のバラツキがある場合もありますが、品質には問題ありません。 ●開封後はお早めにお召し上がりください。","お食事の前に1粒、1日2粒（1回1粒を1日2回）を目安に、水またはぬるま湯とともにお召し上がりください。","【食経験による評価】 当該製品は一日摂取目安量2粒あたり、機能性関与成分であるサラシア由来サラシノールを0.4mg含む錠剤形状の食品である。サラシア由来サラシノールを一日摂取目安量あたり0.8mg含む錠剤形状の類似食品が、平成19年10月から平成27年4月までに293万個以上販売されている。また、サラシア由来サラシノールを一日摂取目安量あたり1.0mg含む錠剤形状の類似食品が、平成19年10月から累計62万個以上出荷されている。上記の類似食品において、これまでに重篤な健康被害は報告されていない。当該製品の機能性関与成分は、類似食品に含まれるサラシア由来サラシノールと同一の成分であり、一日摂取目安量あたりの含有量（サラシア由来サラシノール0.4mg）は、類似食品以下である。また、当該製品と類似食品の剤形は同じ錠剤であり、崩壊性も確認しているため、消化・吸収過程において大きな違いはないものと考える。さらに、当該製品は機能性関与成分に影響を与えるような成分や加工工程を含んでいないことから、機能性関与成分の変質はないものと考える。 以上のことから、類似食品の喫食実績より、当該製品も十分安全な食品であると判断した。 【医薬品との相互作用】 サラシア由来サラシノールには、食後血糖値の上昇をゆるやかにする機能があるため、糖尿病薬との併用には注意が必要である。当該製品の対象者は健常成人であり疾病に罹患している人を対象としていないが、万全を期して、商品パッケージに、摂取上の注意として「糖尿病の薬を服用されている方は、摂取前に医師、薬剤師に相談してください。」と記載し、注意喚起している。なお、これまで糖尿病薬との併用により低血糖が発生したという報告はない。","https://www.fld.caa.go.jp/caaks/s/cssc01/fwccd01?c__id=a09F900004sk8E4IAI","1. 新潟薬科大学 高度薬剤師教育センター サプリメント、健康食品と医療用医薬品の飲み合わせ 2. 城西大学薬学部 食品-医薬品相互作用データベース 3. 独立行政法人 医薬品医療機器総合機構 医療用医薬品の添付文書 4. 厚生労働省 e-ヘルスネット 食物と薬の相互作用","【標題】 サラシア由来サラシノールの食後血糖値の上昇を抑制する機能に関する研究レビュー 【目的】 罹患していない者において、サラシア由来サラシノール（以下サラシノール） の食後血糖値上昇抑制作用を、サラシノールを含まない対照食品（プラセボ）群と比較した臨床試験論文を総合的に評価した研究レビューで明らかにすることを目的とした。 【背景】 サラシノールは、腸の糖類分解酵素であるα-グルコシダーゼの働きを阻害することが分かっている。サラシア由来サラシノールの食後血糖値の上昇を緩やかにする機能については、サラシア属植物普及協会（以下協会）機能性表示ワーキンググループが 2015 年 3 月に作成した研究レビューで評価されているが、その後新しく実施された臨床試験が報告されたことから、研究レビューを最新の情報をもとに更新する必要があった。 【レビュー対象とした研究の特性】 複数のデータベースを用いて、データベース開設あるいは情報搭載時から検索日までを対象とし、2018 年 7 月 6 日～11 日に検索を行った。予め設定した基準に合った論文は 2 編あり、いずれも事実を示す可能性が高いとされる研究方法（ランダム化比較試験）だった。採用された論文 2 編の研究のうち、1 件は協会会員企業の出資によるもので、もう 1 件は協会会員企業が会員となる以前に出資して実施されたものだった。 【主な結果】 採用された論文 2 編はいずれも空腹時血糖値が正常域または境界域（126mg/dL 未満）の疾病に罹患していない日本人（18 歳未満の者、妊産婦、授乳婦は除く）を対象とした研究で、糖質を含む食事1 回あたりサラシノールとして0.03～0.5 mg を摂取したとき、食後血糖値や、食事からの糖の吸収量を示す食後血糖の血中濃度曲線下面積（AUC 0-120 min）がプラセボと比較して減少していた。なお、サラシノールに起因すると考えられる健康被害はなかった。 【科学的根拠の質】 採用された論文 2 編は、いずれもサラシノールを含む製品の販売企業が主宰した試験であり、真の結果と異なる方向に導かれる要因（バイアス）が生じた可能性がある。また、参加者数が少ない、試験の事前登録がされていない、群分け方法の記載がないなど、バイアスを高めてしまう事項も少しあった。しかし、研究レビューの目的に対して、いずれの研究も肯定的で、一貫した結果が得られており、バイアスも基準以下であったことから、今後の研究によって結果が大きく変更される可能性は低いと考えられる。","三生医薬株式会社　大渕工場　静岡県富士市大淵4527-7 三生医薬株式会社　阿幸地工場　静岡県富士宮市阿幸地町334 三生医薬株式会社　依田橋工場　静岡県富士市今泉花の木643-2 三生医薬株式会社　依田橋第二工場　静岡県富士市今泉字三条319-1 三生医薬株式会社　富士根工場　静岡県富士宮市小泉1661-1","当該製品の製造は、GMP適合認定を取得した製造工場で、予め定められた適正な製造基準に従って製造している。","サラシアエキス末","ホームページお問合せフォームから　https://www.fracora.com/index.php/module/Toiawase/action/Toiawase/backflag/0","コールセンター：平日9時～21時　 土日祝9時～17時 ファックス、メール：24時間受付","当該製品中の一般成分を分析した結果、一日摂取目安量2粒あたりの含有量は、脂質：0.01g、炭水化物：0.42g（糖質0.28g/食物繊維0.15g）、ナトリウム：1.2mg（食塩相当量：0.003g）と、脂質及びナトリウム（食塩相当量）は極めて微量であった。また、糖類については、当該製品中の糖質が全て糖類と仮定しても、世界保健機関（WHO）が推奨している糖類の摂取基準※と比較して低い値であった。 ※WHOのガイドラインでは、遊離糖（糖類）を一日に摂取する熱量の10%未満（成人では約50g未満）、望ましくは5%未満（約25g未満）とすることを推奨している。  以上のことから、当該製品の継続的な摂取はもとより、仮に一日摂取目安量以上を摂取した場合でも、健康増進法施行規則第11条第2項で定める栄養素の過剰な摂取につながらないと考えられる。",{"id":263,"documentId":264,"Name":265,"createdAt":266,"updatedAt":267,"publishedAt":268,"FID":269,"ModifyDate":270,"RepealDate":271,"SortNo":272,"RegistDate":273,"Class":28,"ComponentTxt":274,"FunctionFull":275,"SaleStatus":86,"Intake":43,"CategoryName":43,"Extract":34,"ConsumerContact":43,"Website":43,"ResponsibleBureau":43,"Tel":43,"TargetAudience":43,"SalesDate":25,"ModifyHistory20250331":43,"ModifyHistory20250401":43,"ReNotification":34,"IdentityReason":43,"Retraction":34,"RetractionTxt":43,"SelfInspection":43,"SelfInspectionChk1":34,"SelfInspectionChk2":34,"SelfInspectionChk3":34,"ExistingFID":43,"SelfInspectionChk4":34,"IntakeAmount":43,"PrecautionsTake":43,"HowToTake":43,"SafetySelf":43,"EatingResults":43,"FldWebsite":43,"OtherReasons":43,"NonEatingResults":34,"PublicDB2":43,"SafetyEvaluation2":43,"PrimaryInformation3":43,"SafetyEvaluation3":43,"PublicDB4":43,"SafetyEvaluation4":43,"PrimaryInformation5":43,"SafetyEvaluation5":43,"SafetyTest67":43,"ReferenceDB8":43,"Interaction1":43,"ReferenceDB9":43,"Interaction2":43,"ManufacturingSite1":43,"ManufacturingSite2":43,"ManufacturingSite3":43,"ManufacturingSite4":43,"ManufacturingSite5":43,"Location1":43,"Location2":43,"Location3":43,"Location4":43,"Location5":43,"SntermediateProducts1":34,"SntermediateProducts2":34,"SntermediateProducts3":34,"SntermediateProducts4":34,"SntermediateProducts5":34,"FinalProduct1":34,"FinalProduct2":34,"FinalProduct3":34,"FinalProduct4":34,"FinalProduct5":34,"ManufacturingStandards1":34,"ManufacturingStandards2":34,"ManufacturingStandards3":34,"ManufacturingStandards4":34,"ManufacturingStandards5":34,"FunctionSelf":43,"ManufacturingAddress":43,"ManufacturingInfo":43,"RawMaterials":43,"IndicatorComponent":43,"HealthDamage":43,"TelNo":43,"Email":43,"OtherContact":43,"AvailableHours":43,"AcademicConsensus":34,"Identity":34,"HumanTesting":34,"CITNo":43,"PeerReview":34,"TabletPositive":34,"PeerReviewNot":34,"HowToTakeB":34,"HowToSave":43,"SaveInfo1":43,"SaveInfo2":43,"OverdoseInfo":43,"SRproduct":34,"SRcomponent":34,"EatingResultsFinal":34,"EatingResultsSimilar":34,"Equivalence2":34,"Equivalence3":34,"Equivalence4":34,"Equivalence5":34,"PRISMA":43,"IngredientList":25},89550,"py2qty8zhufz32brssw3m2ul","ライラック　ビオ","2025-05-22T13:54:21.776Z","2026-09-28T03:31:04.093Z","2026-09-28T03:31:04.102Z","F26","2022-12-01","2023-05-01",60026,"2020-04-09","有胞子性乳酸菌 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lilac-01が含まれています。便秘傾向の方の便の状態（便の色、臭い、量、形）を整え、お通じ（回数、残便感）を改善することが報告されています。便秘傾向の方に適した食品です。",{"id":277,"documentId":278,"Name":279,"createdAt":280,"updatedAt":281,"publishedAt":282,"FID":283,"ModifyDate":270,"RepealDate":271,"SortNo":284,"RegistDate":285,"Class":28,"ComponentTxt":286,"FunctionFull":287,"SaleStatus":86,"Intake":43,"CategoryName":43,"Extract":34,"ConsumerContact":43,"Website":43,"ResponsibleBureau":43,"Tel":43,"TargetAudience":43,"SalesDate":25,"ModifyHistory20250331":43,"ModifyHistory20250401":43,"ReNotification":34,"IdentityReason":43,"Retraction":34,"RetractionTxt":43,"SelfInspection":43,"SelfInspectionChk1":34,"SelfInspectionChk2":34,"SelfInspectionChk3":34,"ExistingFID":43,"SelfInspectionChk4":34,"IntakeAmount":43,"PrecautionsTake":43,"HowToTake":43,"SafetySelf":43,"EatingResults":43,"FldWebsite":43,"OtherReasons":43,"NonEatingResults":34,"PublicDB2":43,"SafetyEvaluation2":43,"PrimaryInformation3":43,"SafetyEvaluation3":43,"PublicDB4":43,"SafetyEvaluation4":43,"PrimaryInformation5":43,"SafetyEvaluation5":43,"SafetyTest67":43,"ReferenceDB8":43,"Interaction1":43,"ReferenceDB9":43,"Interaction2":43,"ManufacturingSite1":43,"ManufacturingSite2":43,"ManufacturingSite3":43,"ManufacturingSite4":43,"ManufacturingSite5":43,"Location1":43,"Location2":43,"Location3":43,"Location4":43,"Location5":43,"SntermediateProducts1":34,"SntermediateProducts2":34,"SntermediateProducts3":34,"SntermediateProducts4":34,"SntermediateProducts5":34,"FinalProduct1":34,"FinalProduct2":34,"FinalProduct3":34,"FinalProduct4":34,"FinalProduct5":34,"ManufacturingStandards1":34,"ManufacturingStandards2":34,"ManufacturingStandards3":34,"ManufacturingStandards4":34,"ManufacturingStandards5":34,"FunctionSelf":43,"ManufacturingAddress":43,"ManufacturingInfo":43,"RawMaterials":43,"IndicatorComponent":43,"HealthDamage":43,"TelNo":43,"Email":43,"OtherContact":43,"AvailableHours":43,"AcademicConsensus":34,"Identity":34,"HumanTesting":34,"CITNo":43,"PeerReview":34,"TabletPositive":34,"PeerReviewNot":34,"HowToTakeB":34,"HowToSave":43,"SaveInfo1":43,"SaveInfo2":43,"OverdoseInfo":43,"SRproduct":34,"SRcomponent":34,"EatingResultsFinal":34,"EatingResultsSimilar":34,"Equivalence2":34,"Equivalence3":34,"Equivalence4":34,"Equivalence5":34,"PRISMA":43,"IngredientList":25},91123,"v6g6a7d27cjvpsd6rcl0rmcy","夢みるクチナシ","2025-05-22T14:00:38.402Z","2026-09-28T03:42:59.205Z","2026-09-28T03:42:59.213Z","G532",70532,"2021-08-26","クロセチン","本品にはクロセチンが含まれます。クロセチンは、良質な眠りをサポートする（睡眠の質（眠りの深さ）を高め、起床時の眠気や疲労感を和らげる）ことが報告されています。",{"id":289,"documentId":290,"Name":291,"createdAt":292,"updatedAt":293,"publishedAt":294,"FID":295,"ModifyDate":80,"RepealDate":81,"SortNo":296,"RegistDate":297,"Class":28,"ComponentTxt":201,"FunctionFull":298,"SaleStatus":86,"Intake":43,"CategoryName":43,"Extract":34,"ConsumerContact":43,"Website":43,"ResponsibleBureau":43,"Tel":43,"TargetAudience":43,"SalesDate":25,"ModifyHistory20250331":43,"ModifyHistory20250401":43,"ReNotification":34,"IdentityReason":43,"Retraction":34,"RetractionTxt":43,"SelfInspection":43,"SelfInspectionChk1":34,"SelfInspectionChk2":34,"SelfInspectionChk3":34,"ExistingFID":43,"SelfInspectionChk4":34,"IntakeAmount":43,"PrecautionsTake":43,"HowToTake":43,"SafetySelf":43,"EatingResults":43,"FldWebsite":43,"OtherReasons":43,"NonEatingResults":34,"PublicDB2":43,"SafetyEvaluation2":43,"PrimaryInformation3":43,"SafetyEvaluation3":43,"PublicDB4":43,"SafetyEvaluation4":43,"PrimaryInformation5":43,"SafetyEvaluation5":43,"SafetyTest67":43,"ReferenceDB8":43,"Interaction1":43,"ReferenceDB9":43,"Interaction2":43,"ManufacturingSite1":43,"ManufacturingSite2":43,"ManufacturingSite3":43,"ManufacturingSite4":43,"ManufacturingSite5":43,"Location1":43,"Location2":43,"Location3":43,"Location4":43,"Location5":43,"SntermediateProducts1":34,"SntermediateProducts2":34,"SntermediateProducts3":34,"SntermediateProducts4":34,"SntermediateProducts5":34,"FinalProduct1":34,"FinalProduct2":34,"FinalProduct3":34,"FinalProduct4":34,"FinalProduct5":34,"ManufacturingStandards1":34,"ManufacturingStandards2":34,"ManufacturingStandards3":34,"ManufacturingStandards4":34,"ManufacturingStandards5":34,"FunctionSelf":43,"ManufacturingAddress":43,"ManufacturingInfo":43,"RawMaterials":43,"IndicatorComponent":43,"HealthDamage":43,"TelNo":43,"Email":43,"OtherContact":43,"AvailableHours":43,"AcademicConsensus":34,"Identity":34,"HumanTesting":34,"CITNo":43,"PeerReview":34,"TabletPositive":34,"PeerReviewNot":34,"HowToTakeB":34,"HowToSave":43,"SaveInfo1":43,"SaveInfo2":43,"OverdoseInfo":43,"SRproduct":34,"SRcomponent":34,"EatingResultsFinal":34,"EatingResultsSimilar":34,"Equivalence2":34,"Equivalence3":34,"Equivalence4":34,"Equivalence5":34,"PRISMA":43,"IngredientList":25},91979,"me7054mlnegekbkz9sijgxf5","ナチュネル","2025-05-22T14:07:35.323Z","2026-09-28T03:49:31.337Z","2026-09-28T03:49:31.346Z","G1388",71388,"2022-03-17","本品にはL-テアニンが含まれます。L-テアニンには、夜間の睡眠の質を高める（起床時の疲労感や眠気を軽減）ことをサポートすることが報告されています。また、一過性の作業にともなうストレスをやわらげることが報告されています。",{"id":300,"documentId":301,"Name":302,"createdAt":303,"updatedAt":304,"publishedAt":305,"FID":306,"ModifyDate":237,"RepealDate":238,"SortNo":307,"RegistDate":308,"Class":28,"ComponentTxt":309,"FunctionFull":310,"SaleStatus":86,"Intake":311,"CategoryName":312,"Extract":34,"ConsumerContact":35,"Website":245,"ResponsibleBureau":37,"Tel":38,"TargetAudience":313,"SalesDate":314,"ModifyHistory20250331":315,"ModifyHistory20250401":43,"ReNotification":34,"IdentityReason":43,"Retraction":45,"RetractionTxt":248,"SelfInspection":43,"SelfInspectionChk1":34,"SelfInspectionChk2":34,"SelfInspectionChk3":34,"ExistingFID":43,"SelfInspectionChk4":34,"IntakeAmount":316,"PrecautionsTake":317,"HowToTake":318,"SafetySelf":319,"EatingResults":49,"FldWebsite":320,"OtherReasons":43,"NonEatingResults":45,"PublicDB2":70,"SafetyEvaluation2":43,"PrimaryInformation3":70,"SafetyEvaluation3":43,"PublicDB4":70,"SafetyEvaluation4":43,"PrimaryInformation5":49,"SafetyEvaluation5":321,"SafetyTest67":51,"ReferenceDB8":322,"Interaction1":43,"ReferenceDB9":43,"Interaction2":43,"ManufacturingSite1":43,"ManufacturingSite2":43,"ManufacturingSite3":43,"ManufacturingSite4":43,"ManufacturingSite5":43,"Location1":43,"Location2":43,"Location3":43,"Location4":43,"Location5":43,"SntermediateProducts1":34,"SntermediateProducts2":34,"SntermediateProducts3":34,"SntermediateProducts4":34,"SntermediateProducts5":34,"FinalProduct1":34,"FinalProduct2":34,"FinalProduct3":34,"FinalProduct4":34,"FinalProduct5":34,"ManufacturingStandards1":34,"ManufacturingStandards2":34,"ManufacturingStandards3":34,"ManufacturingStandards4":34,"ManufacturingStandards5":34,"FunctionSelf":323,"ManufacturingAddress":324,"ManufacturingInfo":325,"RawMaterials":326,"IndicatorComponent":43,"HealthDamage":66,"TelNo":35,"Email":43,"OtherContact":327,"AvailableHours":68,"AcademicConsensus":45,"Identity":34,"HumanTesting":34,"CITNo":43,"PeerReview":34,"TabletPositive":45,"PeerReviewNot":45,"HowToTakeB":34,"HowToSave":69,"SaveInfo1":70,"SaveInfo2":43,"OverdoseInfo":328,"SRproduct":34,"SRcomponent":45,"EatingResultsFinal":34,"EatingResultsSimilar":34,"Equivalence2":34,"Equivalence3":34,"Equivalence4":34,"Equivalence5":45,"PRISMA":43,"IngredientList":25},92314,"a39r9n621b0v4bay60fzz3jg","疲労ケアＷ","2025-05-22T14:09:40.902Z","2026-09-28T03:52:14.252Z","2026-09-28T03:52:14.261Z","H278",80278,"2022-06-17","ユーグレナグラシリスＥＯＤ－１株由来パラミロン（β－１，３－グルカンとして）","本品にはユーグレナグラシリスＥＯＤ－１株由来パラミロン（β－１，３－グルカンとして）が含まれます。ユーグレナグラシリスＥＯＤ－１株由来パラミロン（β－１，３－グルカンとして）には、日常生活における一時的な精神的・身体的疲労感を軽減する機能があることが報告されています。","350mg","ユーグレナグラシリス・5-アミノレブリン酸リン酸塩含有食品","健康な成人","2022-08-20","（2024.12.26）様式Ⅳの修正","3粒","●本品は、多量摂取により疾病が治癒したり、より健康が増進するものではありません。1日摂取目安量を守ってください。 ●原材料名をご参照の上、食物アレルギーのある方は摂取しないでください。 ●乳幼児の手の届かないところに保管してください。 ●色調等に若干のバラツキがある場合もありますが、品質には問題ありません。 ●開封後はお早めにお召し上がりください。","水またはぬるま湯とともにお召し上がりください。","・本品の機能性関与成分であるユーグレナグラシリスＥＯＤ－１株由来パラミロンを含む食品原料であるユーグレナグラシリスＥＯＤ－１株の乾燥粉末は、日本国内では2017年より販売されています。以降、サプリメント製品や食品に使用されていますが、これまでに有害事象についての報告はありません。  ・機能性関与成分ユーグレナグラシリスＥＯＤ－１株由来パラミロンを含有し、本品に配合されている原材料と同等のユーグレナグラシリスＥＯＤ－１株の乾燥粉末を用いた安全性試験の結果を報告した論文を評価しました。その結果、健常成人を対象に一日摂取目安量を12週間摂取させた長期摂取試験において、ユーグレナグラシリスＥＯＤ－１株の乾燥粉末の摂取に伴う臨床上問題となる変動・有害事象は認められていませんでした。  ・機能性関与成分ユーグレナグラシリスＥＯＤ－１株由来パラミロンを含有し、本品に配合されている原材料と同等のユーグレナグラシリスＥＯＤ－１株の乾燥粉末を用いて安全性試験を実施しました。 ①毒性、遺伝子突然変異誘発性の有無を調べるため、細菌を用いた復帰突然変異試験、ラットを用いた小核試験、ラットを用いた単回経口投与毒性試験、ラットを用いた90日反復投与経口毒性試験、胚・胎児発生に関する試験を実施したところ、何れの試験においても有害性は確認されませんでした。   ②健常成人を対象に一日摂取目安量の約10倍量を4週間摂取させた過剰摂取試験において、ユーグレナグラシリスＥＯＤ－１株の乾燥粉末の摂取に伴う医学的に問題のある変化は認められませんでした。  ・ユーグレナグラシリスＥＯＤ－１株由来パラミロンの医薬品との相互作用に関して有害事象は報告されておりません。  以上のことから、本品を適切に摂取する場合、安全性に問題は無いと考えられます。","https://www.fld.caa.go.jp/caaks/s/cssc01/fwccd01?c__id=a09F900004sk8TfIAI","評価が不十分","１．城西大学　食品－医薬品相互作用データベース　Ver10.0 ２．JDreamⅢ（JSTPlus + JMEDPlus + JST7580）","【標題】ユーグレナグラシリスＥＯＤ－１株由来パラミロンの精神的疲労感および身体的疲労感軽減作用に関する評価  【目的】健康な成人を対象とし、ユーグレナグラシリスＥＯＤ－１株由来パラミロンを含む食品の経口摂取が、ユーグレナグラシリスＥＯＤ－１株由来パラミロンを含まない食品を経口摂取した場合と比較して、精神的疲労感および身体的疲労感を軽減させるかを評価することである。  【背景】これまでにユーグレナグラシリスＥＯＤ－１株由来パラミロンを含む食品の摂取による精神的疲労感や身体的疲労感の軽減作用が報告されているが、それらを総合的に評価した報告はない。  【レビュー対象とした研究の特性】ユーグレナグラシリスＥＯＤ－１株由来パラミロンを含む食品のヒトへの疲労感軽減作用に関する研究を探索した。2021年7月21日に文献検索を実施し、検索日以前にデータベースに登録された日本語および英語の文献を対象とした。評価対象となった文献は2報であり、どちらの研究もランダム化二重盲検プラセボ対照並行群間比較試験であった。  【主な結果】一日当たりユーグレナグラシリスＥＯＤ－１株由来パラミロン350mgを含む食品を摂取することにより、日常生活における精神的疲労や身体的疲労の主観的評価指標や主に精神的疲労の客観的評価指標が軽減されることが明らかとなった。このことから、ユーグレナグラシリスＥＯＤ－１株由来パラミロン350mgを含む食品の摂取は、日常生活の精神的・身体的疲労感を軽減すると考えられた。  【科学的根拠の質】全体を通してバイアスリスクは中程度で、非一貫性はアウトカムにより低～高程度であったが、非直接性、不精確、その他バイアスリスクは低く、総じて研究の妥当性・信頼性は中～高程度と考えられた。但し、対象研究の参加者の選定に偏りがなかったかなど評価できないバイアスがあるといった限界もあった。","三生医薬株式会社　大渕工場　　　　 静岡県富士市大淵4527-7 三生医薬株式会社　阿幸地工場　　　 静岡県富士宮市阿幸地町334 三生医薬株式会社　依田橋工場　　 　静岡県富士市今泉花の木643-2 三生医薬株式会社　依田橋第二工場　 静岡県富士市今泉字三条319-1 三生医薬株式会社　富士根工場　　　 静岡県富士宮市小泉1661-1","本品は、公益財団法人日本健康・栄養食品協会の健康補助食品GMP適合認定を取得した製造工場で製造しており、GMPに準拠した製造および品質管理を行っています。","ユーグレナグラシリス末","ホームページお問合せフォームから","本品中の一般成分を分析した結果、一日摂取目安量3粒あたりの含有量は、脂質：0.03g、炭水化物：0.63g、ナトリウム：2.0mg（食塩相当量：0.005g）と、脂質及びナトリウム（食塩相当量）は極めて微量であった。また、糖類については、本品中の糖質が全て糖類と仮定しても、世界保健機関（WHO）が推奨している糖類の摂取基準※と比較して低い値であった。 ※WHOのガイドラインでは、遊離糖（糖類）を一日に摂取する熱量の10%未満（成人では約50g未満）、望ましくは5%未満（約25g未満）とすることを推奨している。  以上のことから、本品の継続的な摂取はもとより、仮に一日摂取目安量以上を摂取した場合でも、健康増進法施行規則第11条第2項で定める栄養素の過剰な摂取につながらないと考えられる。",{"id":330,"documentId":331,"Name":332,"createdAt":333,"updatedAt":334,"publishedAt":335,"FID":336,"ModifyDate":337,"RepealDate":25,"SortNo":338,"RegistDate":339,"Class":28,"ComponentTxt":340,"FunctionFull":341,"SaleStatus":31,"Intake":342,"CategoryName":343,"Extract":34,"ConsumerContact":35,"Website":344,"ResponsibleBureau":37,"Tel":38,"TargetAudience":345,"SalesDate":346,"ModifyHistory20250331":43,"ModifyHistory20250401":347,"ReNotification":34,"IdentityReason":43,"Retraction":34,"RetractionTxt":43,"SelfInspection":44,"SelfInspectionChk1":45,"SelfInspectionChk2":45,"SelfInspectionChk3":45,"ExistingFID":43,"SelfInspectionChk4":45,"IntakeAmount":348,"PrecautionsTake":349,"HowToTake":318,"SafetySelf":350,"EatingResults":70,"FldWebsite":351,"OtherReasons":43,"NonEatingResults":34,"PublicDB2":49,"SafetyEvaluation2":321,"PrimaryInformation3":49,"SafetyEvaluation3":321,"PublicDB4":49,"SafetyEvaluation4":51,"PrimaryInformation5":43,"SafetyEvaluation5":43,"SafetyTest67":43,"ReferenceDB8":352,"Interaction1":43,"ReferenceDB9":43,"Interaction2":43,"ManufacturingSite1":43,"ManufacturingSite2":43,"ManufacturingSite3":43,"ManufacturingSite4":43,"ManufacturingSite5":43,"Location1":43,"Location2":43,"Location3":43,"Location4":43,"Location5":43,"SntermediateProducts1":34,"SntermediateProducts2":34,"SntermediateProducts3":34,"SntermediateProducts4":34,"SntermediateProducts5":34,"FinalProduct1":34,"FinalProduct2":34,"FinalProduct3":34,"FinalProduct4":34,"FinalProduct5":34,"ManufacturingStandards1":34,"ManufacturingStandards2":34,"ManufacturingStandards3":34,"ManufacturingStandards4":34,"ManufacturingStandards5":34,"FunctionSelf":353,"ManufacturingAddress":354,"ManufacturingInfo":355,"RawMaterials":356,"IndicatorComponent":43,"HealthDamage":66,"TelNo":35,"Email":43,"OtherContact":357,"AvailableHours":358,"AcademicConsensus":34,"Identity":34,"HumanTesting":34,"CITNo":43,"PeerReview":34,"TabletPositive":45,"PeerReviewNot":45,"HowToTakeB":34,"HowToSave":69,"SaveInfo1":70,"SaveInfo2":43,"OverdoseInfo":359,"SRproduct":34,"SRcomponent":45,"EatingResultsFinal":34,"EatingResultsSimilar":34,"Equivalence2":34,"Equivalence3":34,"Equivalence4":45,"Equivalence5":34,"PRISMA":43,"IngredientList":25},78648,"mdsw7qfmry0d6bkjyya41d6j","ＵＶ（ユーブイ）インナープロテクト","2025-05-22T14:25:13.004Z","2026-05-03T06:47:38.466Z","2026-05-03T06:47:38.475Z","J179","2026-05-01",100179,"2024-05-21","アスタキサンチン","本品には、アスタキサンチンが含まれます。抗酸化作用を持つアスタキサンチンは、紫外線刺激から肌を保護するのを助ける機能性、紫外線を浴びた肌を乾燥から守り、肌のうるおいを守る機能性が報告されています。","３mg","アスタキサンチン含有食品","https://www.fld.caa.go.jp/caaks/cssc01/","健常成人男女","2025-03-01","（2025.09.11）様式I 届出書作成に当たっての確認事項、届出後の届出項目、様式VI 表示及び情報開示の在り方に係る事項 （2025.12.19）様式I 届出書作成に当たっての確認事項、届出後の届出項目、様式VI 表示及び情報開示の在り方に係る事項","１粒","・本品は、多量摂取により疾病が治癒したり、より健康が増進するものではありません。1日の摂取目安量を守ってください。 ・原材料名をご参照の上、食物アレルギーのある方は摂取しないでください。 ・乳幼児の手の届かないところに保管してください。 ・色調等に若干のバラツキがある場合もありますが、品質には問題ありません。 ・開封後はお早めにお召し上がりください。","当該製品に含まれるアスタキサンチンの安全性に関しては、以下のものが報告されている。 ・アスタキサンチンは自然界に広く存在し、食品として通常に摂取している。 ・天然由来アスタキサンチンはEU内で複数の製品として 1 日あたり最大12mgの用量で販売されており、世界中の各国の管轄当局によって1日あたり最大24 mgの用量で承認されている。 ・ヒトを対象とした研究では、少なくとも87の臨床試験において、2,000名以上が参加し、短期摂取（最大100mg）および長期摂取（平均8～12mg）のいずれにおいても、天然アスタキサンチンによる重篤な有害事象は確認されていない。 ・入手可能な規制データ、前臨床データ、臨床データを考慮すると、少なくとも12mg/日の摂取量での天然由来のアスタキサンチンサプリメントには安全性に関する懸念はない。 なお、アスタキサンチンは固有の化学構造（化学式：C40H52O4）を有する成分であり、本品は合成品ではなく、天然由来のアスタキサンチンのため、上記結果における成分と本品中の機能性関与成分は同等であると判断した。 以上の結果より、機能性関与成分であるアスタキサンチン摂取の安全性に関して問題はないと考えられる。","https://www.fld.caa.go.jp/caaks/s/cssc01/fwccd01?c__id=a09F900004sk7wuIAA","城西大学薬学部 食品‐ 医薬品相互作用データベース（Ver.10.0）","【標題】 機能性関与成分アスタキサンチンの摂取による紫外線に対する肌の維持・改善機能（紫外線から肌を保護し、肌を保湿する機能）に関する研究レビュー  【目的】 健常成人において、アスタキサンチンの摂取は紫外線に対する肌の維持・改善機能を有するかを明らかににするため、定性的研究レビューを実施し、検証することを目的とした。  【背景】 アスタキサンチンは、魚介類などに多く含有されるカロテノイドの一種で、強い抗酸化力をもつことが報告されている。また、ヒトへの機能性としても食品として摂取することで、健常成人の紫外線に対して肌を維持・改善する機能（紫外線から肌を保護し、肌を保湿する機能）が報告されている。 そこで今回、これらの背景を踏まえ、健常成人がアスタキサンチン含有食品を摂取することで、紫外線に対して肌を維持・改善する機能がみられるか、研究レビューを実施した。  【レビュー対象とした研究の特性】 本研究のデザインは、研究レビューであり、5つの電子データベースを使用し、アスタキサンチンを用いて紫外線に対する肌の維持・改善機能について調査したランダム化比較試験（RCT）を収集した。評価項目「紫外線照射からの肌の保護」「紫外線照射からの肌の保湿」について、アスタキサンチン摂取群と対照群のデータについて調査・評価を行った。  【主な結果】 本研究レビューにおいては、アスタキサンチン3-4㎎/dayを摂取した際の紫外線に対して肌を維持・改善する機能に関する評価項目として「紫外線照射からの肌の保護」「紫外線照射からの肌の保湿」を評価している2報の論文が採択されたが、いずれの評価項目においても、過半数を超える論文でプラセボ群と比較してアスタキサンチン群における有意差が確認された。以上より、全研究の過半数を上回る研究において肯定的な結果が得られたことから、紫外線に対して肌を維持・改善する機能が認められたと判断した。　  【科学的根拠の質】 本研究における結果の限界・問題点としては、英語および日本語の論文のみを抽出対象としていることから、他の言語における本研究レビューに関連する論文の存在は否定できず、言語バイアスについて否定できない。また定性的レビューのみ実施しており、メタアナリシスによる検証がなされていない。これにより「非一貫性」や「その他出版バイアスなど」に関する基準が明確となっていないことが挙げられる。","【製造所１】ウキシマメディカル株式会社 　　　　　　静岡県富士市中里2626-65  【製造所２】株式会社ミズ・バラエティー　クリーンルーム棟 　　　　　　静岡県富士市今泉409-1","当該製品の製造は、GMP適合認定、ISO22000を取得した製造工場で、予め定められた適正な製造基準に従って製造している。\n【製造所１】\nウキシマメディカル株式会社\n◆GMP認証取得（日健栄協GMP：30921）\n　　ISO 22000（日本科学技術連盟： JUSE-FS-055）\n\n【製造所２】\n　株式会社ミズ・バラエティー クリーンルーム棟\n　　◆GMP認証取得（日本健康食品規格協会：製-0037）\n","へマトコッカス藻色素","ホームページお問い合わせから","コールセンター：平日：9時～21時 　土日祝：9時～17時 ファックス、メール：24時間受付","本品中の一般成分を分析した結果、1日摂取目安量1粒あたりの含有量は、脂質：0.23g、炭水化物：0.03g、食塩相当量：0.0011g(ナトリウム：約0.4mg)となった。脂質については1日摂取目安量当たり0.23gであるため、過剰摂取に繋がることはない。糖類については、本品中の炭水化物をすべて糖類と仮定しても、世界保健機関（WHO）が推奨している糖類の摂取基準※1と比較して低い値であった。また、ナトリウムについても日本人の食事摂取基準(2020年版)※2と比較して低い値であった。 以上より、本品の継続的な摂取及び仮に1日摂取目安量以上の摂取した場合でも、健康増進法施行規則第11条第2項で定められる栄養素の過剰な摂取に繋がらないと考えられる。  ※1　WHO推奨の糖類の摂取基準 日本での摂取基準は設定されていない。WHOのガイドラインでは遊離糖(糖類)の摂取量を、1日に摂取する熱量の10%未満(成人で約50g未満)、望ましくは5%未満(約25g未満)とすることを推奨。  ※2　日本人の食事摂取基準(2020年版) 成人男性は7.5g未満、成人女性は6.5g未満の目標量が設定されている。",{"pagination":361},{"page":362,"pageSize":363,"pageCount":362,"total":362},1,25,1790614449465]