Label: KENKODERM PSORIASIS MOISTURIZING- salicylic acid cream
- NDC Code(s): 73632-004-01
- Packager: Olympus Trading Company, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 12, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only
Ask a doctor before use if you have:
- ▪
- a condition that covers a large area of the body
- ▪
- an allergy or sensitivity to Salicylic Acid
Stop use and ask a doctor if
condition worsens or does not improve after regular use of this product as directed.
- Directions
- Other information
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Inactive ingredients
Water (Aqua), Urea, Propylene Glycol, Glyceryl Stearate SE, Cetearyl Alcohol, Butyrospermum Parkii (Shea) Butter, Limnanthes Alba (Meadowfoam) Seed Oil, Glycerin, Cetyl Alcohol, Glyceryl Stearate, PEG-100 Stearate, Behentrimonium Methosulfate, Sodium Hyaluronate, Niacinamide, Ceramide NP, Ceramide AP, Ceramide EOP, Tocopherol, Phytosphingosine, Cholesterol, Sodium Lauroyl Lactylate, Dimethicone, Carbomer, Xanthan Gum, Phenoxyethanol, Disodium EDTA, Ethylhexylglycerin, Sodium Hydroxide
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INGREDIENTS AND APPEARANCE
KENKODERM PSORIASIS MOISTURIZING
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73632-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) UREA (UNII: 8W8T17847W) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) SHEA BUTTER (UNII: K49155WL9Y) MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y) GLYCERIN (UNII: PDC6A3C0OX) CETYL ALCOHOL (UNII: 936JST6JCN) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61) HYALURONATE SODIUM (UNII: YSE9PPT4TH) NIACINAMIDE (UNII: 25X51I8RD4) CERAMIDE NP (UNII: 4370DF050B) CERAMIDE 1 (UNII: 5THT33P7X7) TOCOPHEROL (UNII: R0ZB2556P8) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) CHOLESTEROL (UNII: 97C5T2UQ7J) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) DIMETHICONE (UNII: 92RU3N3Y1O) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) XANTHAN GUM (UNII: TTV12P4NEE) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73632-004-01 295 g in 1 JAR; Type 0: Not a Combination Product 08/05/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 08/05/2020 Labeler - Olympus Trading Company, LLC (037947326) Establishment Name Address ID/FEI Business Operations Fragrance Manufacturing, Inc. 793406000 MANUFACTURE(73632-004)