Label: W.SKIN CICA PLUS REPAIR- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 74997-0010-1 - Packager: J&J COMPANY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated April 24, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Butylene Glycol, Caprylic/Capric Triglyceride, Glycerin, Niacinamide, Betaine, Polyglyceryl-3 Methylglucose Distearate, Cetyl Alcohol, Butyrospermum Parkii (Shea) Butter, Glyceryl Stearate, Trehalose, Ammonium Acryloyldimethyltaurate/VP Copolymer, Glyceryl Caprylate, Glyceryl Stearate Citrate, Stearyl Alcohol, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyisobutene, Chlorphenesin, Myristyl Alcohol, Allantoin, Fragrance, Panthenol, Adenosine, Lauryl Alcohol, Caprylyl/Capryl Glucoside, Sorbitan Oleate, Disodium EDTA, Centella Asiatica Extract, Acacia Senegal Gum, Citric Acid, Peat Water, Hydroxypropyl Methylcellulose, 1,2-Hexanediol, Portulaca Oleracea Extract, Pentylene Glycol, Caprylyl Glycol, Potassium Sorbate
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
W.SKIN CICA PLUS REPAIR
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74997-0010 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 ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74997-0010-1 50 mL in 1 TUBE; Type 0: Not a Combination Product 04/25/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/25/2021 Labeler - J&J COMPANY (688995236) Registrant - J&J COMPANY (688995236) Establishment Name Address ID/FEI Business Operations J&J COMPANY 688995236 manufacture(74997-0010) , label(74997-0010) , pack(74997-0010)