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GeriTaiwan's FDA to Regulate Health Food Claims for 17 Ingredients
Taiwan's FDA to Regulate Health Food Claims for 17 Ingredients
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自由时报04.06.2026Sağlık2 dk okumaChina

Taiwan's FDA to Regulate Health Food Claims for 17 Ingredients

Hızlı Bakış

Taiwan's FDA is planning new regulations to restrict functional claims for 17 health food ingredients, requiring product registration and adherence to approved wording to combat misleading marketing and enhance transparency.

Yapay zekâ özeti

Neden Önemli?

Taiwan's FDA currently manages 14 health food categories with a 'little green man' logo for approved products. However, many products use borderline language for claims, creating a market gray area. The FDA plans to regulate functional claims for 17 specific ingredients.

Yazı boyutu

市售保健食品眾多,目前食藥署針對14項保健功效產品進行嚴格管理,並核發「小綠人標章」(可宣稱特定保健功效),但近年有許多產品用詞遊走於法律邊緣,衛福部食藥署規劃針對17項功能性原料或成分,限制對應的功能詞句,並要求業者完成相關登錄程序,但新制仍在規劃中,尚無確切上路時間。

目前衛福部公告的健康食品保健功效共有14項,包括「骨質保健、調節血脂、胃腸功能改善、免疫調節、牙齒保健、護肝、調節血糖、延緩衰老、抗疲勞、輔助調節血鐵、輔助調節血壓、不易形成體脂肪、輔助調整過敏體質及膝關節保健」等。

食藥署企劃及科技管理組長鄭維智表示,現行「健康食品」經過嚴格的安全性與功效評估(查驗登記),並具備實質科學證據,審查通過後,可取得「小綠人標章」,可宣稱特定保健功效,除此類食品以外,都視為「一般食品」,但近年來有許多產品以遊走法規邊緣的話術進行宣稱,產生市場灰色地帶。

鄭維智指出,參考日、韓、歐盟等國際先進國家規範,食藥署擬針對17項功能性原料或成分,明定可敘述的功能性詞句,且業者若想進行相關功能性宣稱,須先至指定平台進行產品登錄,取得登錄字號,並依規定上傳其功能性成分含量符合宣稱詞句的科學參考資料。

17項功能性原料或成分包括葉黃素、難消化性糊精、菊糖、益生菌/乳酸菌、GABA、 EPA及DHA、葡萄糖胺、膠原蛋白、肌酸、含兒茶素之綠茶萃取物、β-聚葡萄糖、人參、紅參、果寡糖、α-環狀糊精、幾丁聚糖、植物固醇等。

鄭維智說,未來業者除依規定辦理產品登錄外,也要明確揭露功能性成分或原料、成分含量、功能詞句、適用對象及建議用量,且產品的標示與廣告必須嚴格遵循食藥署「正面表列」的得敘述功能詞句,不得自行衍生或誇大,以強化產品資訊透明度及後市場管理。

食藥署強調,食品不得涉及不實、誇張或易生誤解之宣稱,食品與藥品管理仍應明確區隔,食藥署將持續蒐集各界意見並滾動式修正法規,目前規劃在現行「食安法」架構下進行修訂,透過法規命令層級進行調整,原則上不需修訂母法或另訂專法,目前政策尚無確切上路時間,但食藥署正積極辦理中。

Bundan Sonra Ne Olabilir?

Yapay zekâ öngörüsü — kesinlik taşımaz

  • The FDA will finalize and implement regulations for functional claims on 17 health food ingredients.

    Muhtemel · Aylar içinde

Açık Sorular

  • What is the exact timeline for the new regulations to be implemented?
  • What are the specific penalties for non-compliance?
  • Will existing products need to be re-evaluated or re-registered?
  • How will the FDA monitor and enforce the 'positive list' of approved functional wording?

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