Label: CLEAN AND CLEAR ESSENTIALS DEEP CLEANING ASTRINGENT- salicylic acid liquid
- NDC Code(s): 69968-0209-8
- Packager: Johnson & Johnson Consumer 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 January 5, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- USE
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WARNINGS
For external use only.
Flammable: Keep away from fire or flame.
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DIRECTIONS
- cleanse skin thoroughly before applying this product
- moisten a cotton ball and cover the entire effected area with a thin layer 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 drying or peeling occurs, reduce application to once a day or every other day.
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 240 mL Bottle Label
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INGREDIENTS AND APPEARANCE
CLEAN AND CLEAR ESSENTIALS DEEP CLEANING ASTRINGENT
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0209 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) ISOCETETH-20 (UNII: O020065R7Z) SULISOBENZONE (UNII: 1W6L629B4K) FD&C RED NO. 4 (UNII: X3W0AM1JLX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0209-8 240 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/30/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 04/30/2012 Labeler - Johnson & Johnson Consumer Inc. (118772437)