Label: SALICYLIC ACID- astringent liquid
- NDC Code(s): 36800-875-34
- Packager: TOPCO ASSOCIATES LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 31, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Keep out of reach of children.
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Directions
- clean the skin thoroughly before applying this product
- cover the entire affected area with a thin layer and rinse thoroughly one to three times daily
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce daily application to once a day or every other day
- Inactive ingredients
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SPL UNCLASSIFIED SECTION
*This product is not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of Clean & Clear Sensitive Skin Deep Cleaning Astringent.
Visit us here for more information: http://topbrands.com
DISTRIBUTED BY TOPCO ASSOCIATES LLC
150 NORTHEST POINT BOULEVARD
ELK GROVE VILLAGE, IL 60007
1-888-423-0139 TOPCO VIJA0119
topcare@ topco.com
875.002/875AD-AE
- principal display panel
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID
astringent liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:36800-875 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) ALOE (UNII: V5VD430YW9) BENZOPHENONE (UNII: 701M4TTV9O) DENATONIUM BENZOATE (UNII: 4YK5Z54AT2) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) ISOCETETH-20 (UNII: O020065R7Z) POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A) SODIUM CITRATE (UNII: 1Q73Q2JULR) WATER (UNII: 059QF0KO0R) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36800-875-34 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 06/01/2009 Labeler - TOPCO ASSOCIATES LLC (006935977) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(36800-875) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(36800-875)