Label: SALICYLIC ACID- astringent liquid
- NDC Code(s): 36800-875-34
- 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.
Updated March 7, 2022
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- Active ingredient
- When using this product
- Keep out of reach of children.
- 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
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.
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DISTRIBUTED BY TOPCO ASSOCIATES LLC
150 NORTHEST POINT BOULEVARD
ELK GROVE VILLAGE, IL 60007
1-888-423-0139 TOPCO VIJA0119
- principal display panel
INGREDIENTS AND APPEARANCE
Product 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 final part333D 06/01/2009 Labeler - TOPCO ASSOCIATES LLC (006935977)