Label: W.SKIN CICA FOOT PEELING- milk protein extract liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 74997-0020-1 - 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 May 8, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Stearic Acid, Lauric Acid, Glycerin, Myristic Acid, Potassium Hydroxide, Cocamidopropyl Betaine, Glycol Distearate, Milk Extract, Milk Protein Extract, Hydrolyzed Collagen, Centella Asiatica Extract, Fructan, Oryza Sativa (Rice) Extract, Glycine Soja (Soybean) Seed Extract, Sesamum Indicum (Sesame) Seed Extract, Vaccinium Angustifolium (Blueberry) Fruit Extract, Phaseolus Angularis Seed Extract, Solanum Melongena (Eggplant) Fruit Extract, Arctium Lappa Root Extract, Laminaria Japonica Extract, Undaria Pinnatifida Extract, Butylene glycol, Boswellia Carterii Resin Extract, Geranium Maculatum Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Cymbopogon Schoenanthus Extract, Melissa Officinalis Leaf Extract, Calendula Officinalis Flower Extract, Salvia Officinalis (Sage) Leaf Extract, Monarda Didyma Leaf Extract, Artemisia Princeps Leaf Extract, PEG-100 Stearate, Glyceryl Stearate, PEG-40 Hydrogenated Castor Oil, 1,2-Hexanediol, Sodium Benzoate, Disodium EDTA
- 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 FOOT PEELING
milk protein extract liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74997-0020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CASEIN (UNII: 48268V50D5) (CASEIN - UNII:48268V50D5) CASEIN 0.1 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74997-0020-1 120 mL in 1 TUBE; Type 0: Not a Combination Product 05/08/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/08/2021 Labeler - J&J COMPANY (688995236) Registrant - J&J COMPANY (688995236) Establishment Name Address ID/FEI Business Operations J&J COMPANY 688995236 manufacture(74997-0020) , label(74997-0020) , pack(74997-0020)
