Label: DIAPIA ADL EVER-CURECREAM- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71857-0010-1 - Packager: BSG H & B Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Glycerin, Centella Asiatica Extract, Hydrogenated Polydecene, 1,2-Hexanediol, Butylene Glycol, Cetearyl Alcohol, Polyacrylate-13, Polyisobutene, Polysorbate 20, Polysorbate 60, C13-14 Isoparaffin, Dimethicone, Sodium Polyacrylate, Simmondsia Chinensis (Jojoba) Seed Oil, Olea Europaea (Olive) Fruit Oil, Helianthus Annuus (Sunflower) Seed Oil, Betaine, Macadamia Ternifolia Seed Oil, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Phenoxyethanol, Xanthan Gum, Triethanolamine, Disodium EDTA, Curcuma Longa (Turmeric) Root Powder, Curcuma Longa (Turmeric) Root Extract, Portulaca Oleracea Extract
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DIAPIA ADL EVER-CURECREAM
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71857-0010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL 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:71857-0010-1 30 mL in 1 BOTTLE; 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(71857-0010) , label(71857-0010)
