Label: MEDICATED APRICOT SCRUB- salicylic acid gel
- NDC Code(s): 72476-044-30
- Packager: Retail Business Services, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Keep out of reach of children.
- Directions
- Other information
-
Inactive ingredients
water, Juglans regia (walnut) shell powder, glyceryl stearate SE, glycerin, cetearyl alcohol, cetyl alcohol, decyl glucoside, Zea mays (corn) kernel meal, sodium hydroxide, cocamidopropyl betaine, glyceryl stearate, PEG-100 stearate, Prunus armeniaca (apricot) fruit extract, ceteareth-20, carbomer, polysorbate 60, fragrance, PPG-2 methyl ether, phenethyl alcohol, methylisothiazolinone, benzyl alcohol, limonene, titanium dioxide
- Disclaimer
- SPL UNCLASSIFIED SECTION
- Principal display panel
-
INGREDIENTS AND APPEARANCE
MEDICATED APRICOT SCRUB
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72476-044 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 19.8 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) JUGLANS REGIA SHELL (UNII: PJ10MT7VKA) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) GLYCERIN (UNII: PDC6A3C0OX) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ALCOHOL (UNII: 936JST6JCN) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) CORN GRAIN (UNII: C1Z9U7094Z) SODIUM HYDROXIDE (UNII: 55X04QC32I) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) APRICOT (UNII: 269CJD5GZ9) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) POLYSORBATE 60 (UNII: CAL22UVI4M) PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N) PHENYLETHYL ALCOHOL (UNII: ML9LGA7468) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) BENZYL ALCOHOL (UNII: LKG8494WBH) LIMONENE, (+)- (UNII: GFD7C86Q1W) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72476-044-30 170 g in 1 TUBE; Type 0: Not a Combination Product 12/14/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 12/14/2010 Labeler - Retail Business Services, LLC (967989935) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(72476-044)