Label: CLEAR PROOF BLEMISH CONTROL TONER ACNE MEDICATION- salicylic acid liquid
- NDC Code(s): 51531-6743-5, 51531-6743-9
- Packager: Mary Kay 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 September 23, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Uses
- Warnings
-
Directions
- clean the skin thoroughly before applying this product
- cover the entire affected 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 dryness or peeling occurs, reduce application to once a day or every other day
- Inactive ingredients
- Principal Display Panel - 147 mL bottle
-
INGREDIENTS AND APPEARANCE
CLEAR PROOF BLEMISH CONTROL TONER ACNE MEDICATION
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51531-6743 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) DENATONIUM BENZOATE (UNII: 4YK5Z54AT2) TERT-BUTYL ALCOHOL (UNII: MD83SFE959) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DOCUSATE SODIUM (UNII: F05Q2T2JA0) EUCALYPTUS OIL (UNII: 2R04ONI662) MENTHOL (UNII: L7T10EIP3A) DIMETHICONE (UNII: 92RU3N3Y1O) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51531-6743-5 1 in 1 CARTON 08/15/2013 1 147 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:51531-6743-9 26 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/15/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M006 08/15/2013 Labeler - Mary Kay Inc. (049994452) Establishment Name Address ID/FEI Business Operations Port Jervis Laboratories Inc. 001535103 manufacture(51531-6743) Establishment Name Address ID/FEI Business Operations Mary Kay Inc. 103978839 manufacture(51531-6743)