CLEAR PROOF BLEMISH CONTROL TONER ACNE MEDICATION- salicylic acid liquid 
Mary Kay Inc.

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.

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Clear Proof Blemish Control Toner

Drug Facts

Active ingredient

Salicylic Acid (2% W/W)

Purpose

Acne Medication

Uses

Warnings

For external use only

When using this product

  • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
  • avoid contact with the eyes

Stop use and ask a doctor

if irritation or sensitivity develops or increases

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

alcohol denat., citric acid, diethylhexyl sodium sulfosuccinate, eucalyptus globulus leaf oil, menthol, propylene glycol, simethicone, water

Principal Display Panel - 147 mL bottle

clearproof

blemish control toner

acne medication

2% salicylic acid

liquid

5 FL. OZ. / 147 mL

Mary Kay

image of carton

CLEAR PROOF BLEMISH CONTROL TONER  ACNE MEDICATION
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51531-6743
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51531-6743-51 in 1 CARTON08/15/2013
1147 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:51531-6743-926 mL in 1 BOTTLE; Type 0: Not a Combination Product08/15/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM00608/15/2013
Labeler - Mary Kay Inc. (049994452)
Establishment
NameAddressID/FEIBusiness Operations
Port Jervis Laboratories Inc.001535103manufacture(51531-6743)
Establishment
NameAddressID/FEIBusiness Operations
Mary Kay Inc.103978839manufacture(51531-6743)

Revised: 9/2022
Document Id: e95a84ea-0cd2-27a8-e053-2995a90ae78c
Set id: 22ead982-2073-4df2-bc18-a2389f9425dd
Version: 6
Effective Time: 20220923
 
Mary Kay Inc.