Label: SALICYLIC ACID- astringent liquid
- NDC Code(s): 69842-775-34
- Packager: CVS Pharmacy, Inc
- 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 October 3, 2023
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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.
Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
(c) 2015 CVS/pharmacy
CVS.com 1-800-SHOP CVS
Made in the USA with US and foreign components
DSP-TN-15000 DSP-MO-34 SDS-TN-15012
- principal display panel
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID
astringent liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-775 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) LAMINARIA DIGITATA (UNII: 15E7C67EE8) 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:69842-775-34 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/05/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 06/05/2009 Labeler - CVS Pharmacy, Inc (062312574)