DIAPIA COLLAGEN GOAT MILK AMPOULE MASK- niacinamide liquid 
BSG H & B Co., Ltd.

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.

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Drug Facts

Niacinamide

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

Brightening, Nourishing, Moisturizing, Improving skin elasticity

keep out of reach of the children

Cleanse and dry face thoroughly.

Open pouch, unfold mask and apply to face.

Leave it for 10 - 20 minutes, remove the mask and tap slightly until essence

absorbed.

1.Keep out of reach of children.

2.Store in a cool, dry place and avoid direct sunlight.

3.If abnormal symptoms occur after use, stop use and consult with a skin specialist.

for external use only

label

DIAPIA COLLAGEN GOAT MILK AMPOULE MASK 
niacinamide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71857-0012
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71857-0012-133 g in 1 POUCH; Type 0: Not a Combination Product10/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/30/2020
Labeler - BSG H & B Co., Ltd. (694252895)
Registrant - BSG H & B Co., Ltd. (694252895)
Establishment
NameAddressID/FEIBusiness Operations
BSG H & B Co., Ltd.694252895manufacture(71857-0012) , label(71857-0012)

Revised: 10/2020
Document Id: b2da246c-4b89-7d60-e053-2995a90af50b
Set id: b2da246c-4b88-7d60-e053-2995a90af50b
Version: 1
Effective Time: 20201029
 
BSG H & B Co., Ltd.