Label: MEDICATED APRICOT SCRUB- salicylic acid gel
- NDC Code(s): 36800-009-30
- Packager: Topco Associates LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 7, 2022
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Keep out of reach of children.
- Directions
- Other information
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Inactive ingredients
water, Juglans regia (walnut) shell powder, glyceryl stearate SE, glycerin, decyl glucoside, Zea mays (corn) kernel meal, cetearyl alcohol, cetyl alcohol, triethanolamine, cocamidopropyl betaine, glyceryl stearate, PEG-100 stearate, Prunus armeniaca (apricot) fruit extract, cetyl acetate, ceteareth-20, carbomer, polysorbate 60, acetylated lanolin alcohol, fragrance, PPG-2 methyl ether, phenethyl alcohol, methylisothiazolinone, titanium dioxide
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SPL UNCLASSIFIED SECTION
*This product is not manufactured or distributed by St. Ives Laboratories, distributor of St. Ives Blemish Control Apricot Scrub
DISTRIBUTED BY TOPCO ASSOCIATES LLC
ELK GROVE VILLAGE, IL 60007
1-888-423-0139
topcare@topco.com www.topcarebrand.comThis TopCare product is laboratory tested to guarantee its ightes quality. Your total satisfaction is guaranteed
QUALITY GUARANTEED
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INGREDIENTS AND APPEARANCE
MEDICATED APRICOT SCRUB
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:36800-009 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) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) CORN GRAIN (UNII: C1Z9U7094Z) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ALCOHOL (UNII: 936JST6JCN) trolamine (UNII: 9O3K93S3TK) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) APRICOT (UNII: 269CJD5GZ9) CETYL ACETATE (UNII: 4Q43814HXS) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L) POLYSORBATE 60 (UNII: CAL22UVI4M) ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P) PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N) .ALPHA.-ISOBUTYLPHENETHYL ALCOHOL (UNII: 2SBL0E1I0N) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36800-009-30 170 g in 1 TUBE; Type 0: Not a Combination Product 10/14/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 10/14/2009 Labeler - Topco Associates LLC (006935977)