Label: DIAPIA HA AQUA SHINING MASK- niacinamide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71857-0019-1, 71857-0019-2 - 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
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water
Methylpropanediol
Glycerin
Water
Glycereth-26
Butylene Glycol
PEG/PPG-17/6 Copolymer
Water
Hydroxyethyl Urea
1,2-Hexanediol
Phenoxyethanol
Triethanolamine
Water
Water
Butylene Glycol
Sodium Hyaluronate
Phenoxyethanol
Saccharide Isomerate
Water
Sodium Citrate
Citric Acid
PPG-26-Buteth-26
PEG-40 Hydrogenated Castor Oil
Water
Dipotassium Glycyrrhizate
Carbomer
Allantoin
Hydroxyethylcellulose
Sodium Nitrate
Xanthan Gum
Water
Butylene Glycol
Vaccinium Angustifolium (Blueberry) Fruit Extract
Rubus Idaeus (Raspberry) Fruit Extract
Rubus Fruticosus (Blackberry) Fruit Extract
Euterpe Oleracea Fruit Extract
Fragaria Chiloensis (Strawberry) Fruit Extract
Phenoxyethanol
Water
Aloe Barbadensis Leaf Extract
Butylene Glycol
Phenoxyethanol
Water
Camellia Sinensis Leaf Extract
Butylene Glycol
Phenoxyethanol
Tetrasodium EDTA
Parfum
Polyglutamic Acid
Water - 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:71857-0019 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:71857-0019-2 5 in 1 BOX 12/01/2021 1 NDC:71857-0019-1 24 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/01/2021 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 label(71857-0019) , manufacture(71857-0019)