Label: W.SKIN CICA FOOT PEELING- centella asiatica extract, urea liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 74997-0018-1 - Packager: J&J COMPANY
- 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 May 7, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Glycerin, Carbomer, Steartrimonium Methosulfate, Alcohol, Urea, Centella Asiatica Extract, Citrus Aurantium Dulcis (Orange) Fruit Extract, Daucus Carota Sativa (Carrot) Root Extract, Citrullus Vulgaris (Watermelon) Fruit Extract, Solanum Lycopersicum (Tomato) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Fragaria Ananassa (Strawberry) Fruit Extract, Prunus Serotina (Wild Cherry) Fruit Extract, Rubus Idaeus (Raspberry) Fruit Extract, Prunus Salicina Fruit Extract, Vaccinium Macrocarpon (Cranberry) Fruit Extract, Punica Granatum Fruit Extract, Citrus Paradisi (Grapefruit) Seed Extract, Capsicum Annuum Fruit Extract, Capsicum Annuum Extract, Psidium Guajava Fruit Extract, Wine Extract, Milk Extract, Sodium Hyaluronate, Isopropyl Alcohol , PEG-60 Hydrogenated Castor Oil, 1,2-Hexanediol, Sodium Chloride, Phenoxyethanol, Disodium EDTA, Fragrance
- 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
centella asiatica extract, urea liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74997-0018 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CENTELLA ASIATICA (UNII: 7M867G6T1U) (CENTELLA ASIATICA - UNII:7M867G6T1U) CENTELLA ASIATICA 0.01 g in 100 mL UREA (UNII: 8W8T17847W) (UREA - UNII:8W8T17847W) UREA 0.2 g in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74997-0018-1 200 mL in 1 BOTTLE; 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(74997-0018) , label(74997-0018) , pack(74997-0018)
