Label: DIAPIA COLLAGEN GOAT MILK AMPOULE MASK- niacinamide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71857-0012-1 - Packager: BSG H & B Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated December 10, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Butylene Glycol, Glycerin, Caprylic/Capric Triglyceride, Dimethicone, Cetyl Ethylhexanoate, 1,2-Hexanediol, Polysorbate 60, Hydrogenetaed Polydecene, Ammonium Acryloyldimethyltaurate/VP Copolymer, Phenoxyethanol, Glyceryl Stearate, PEG-100 Stearate, Goat Milk Extract, Xanthan Gum, Ethylhexylglycerin, Sodium Polyacrylate, Disodium EDTA, Fragrance, Melaleuca Alternifolia (Tea Tree) Leaf Water, Buthylphenyl Methylpropional, Silk Amino Acids, Beta-Glucan, Hydrolyzed Collagen, Hydrolyzed Elastin, Citrus Unshiu Peel Extract, Ribes Nigrum (Black Current) Fruit Extract, Vaccinium Angustifolium (Blueberry) Fruit Extract, Lavandula Angustifolia (Lavender) Extract, Rosmarinus Officinalis (Rosemary) Extract, Salvia Officinalis (Sage) Extract, Chamomilla Recutita (Matricaria) Flower Extract, Mentha Piperita (Peppermint) Extract, Ubiquinone, Palmitoyl Tripeptide-5, Acetyl Hexapeptide-8
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DIAPIA COLLAGEN GOAT MILK AMPOULE MASK
niacinamide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71857-0012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71857-0012-1 33 g in 1 POUCH; Type 0: Not a Combination Product 10/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/30/2020 Labeler - BSG H & B Co., Ltd. (694252895) Registrant - BSG H & B Co., Ltd. (694252895) Establishment Name Address ID/FEI Business Operations BSG H & B Co., Ltd. 694252895 manufacture(71857-0012) , label(71857-0012)
