- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Keep out of reach of children.
-
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
-
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
-
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)