Label: DIAPIA HA AQUA SHINING MASK- niacinamide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71857-0013-1 - 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 October 29, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Butylene Glycol, Glycereth-26, Glycerin, Methylpropanediol, 1,2-Hexanediol, Phenoxyethanol, Carbomer, Hydroxyethyl Urea, Triethanolamine, Dipotassium Glycyrrhizate, Allantoin, PEG/PPG-17/6 Copolymer, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Saccharide Isomerate, Xanthan Gum, Tetrasodium EDTA, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Sodium Hyaluronate, Vaccinium Angustifolium (Blueberry) Fruit Extract,
Rubus Idaeus (Raspberry) Fruit Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Euterpe Oleracea Fruit Extract, Fragaria Chiloensis (Strawberry) Fruit Extract, Fragrance, Sodium Citrate, Citric Acid, Polyglutamic Acid, Hydroxyethylcellulose
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DIAPIA HA AQUA SHINING MASK
niacinamide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71857-0013 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 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71857-0013-1 24 mL 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(71857-0013) , label(71857-0013)