CLEAR MED  10%- benzoyl peroxide lotion 
CONTROL CORRECTIVE SKINCARE 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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CONTROL CORRECTION - CLEAR MED 10% (70764-107)

ACTIVE INGREDIENTS

BENZOYL PEROXIDE 10%

PURPOSE

ACNE TREATMENT

USE

HELPS REDUCE ACNE BREAKOUTS.

WARNINGS

FOR EXTERNAL USE ONLY. DO NOT USE IF YOU ARE ALLERGIC OR SENSITIVE TO BENZOYL PEROXIDE. WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES, LIPS AND MOUTH. IF CONTACT OCCURS, FLUSH THOROUGHLY WITH WATER. AVOID UNNECESSARY SUN EXPOSURE. MAY BLEACH FABRIC. MILD IRRITATION MAY BE REDUCED BY USING THE PRODUCT LESS FREQUENTLY OR IN A LOWER CONCENTRATION. DISCONTINUE USE, IF IRRITATION OCCURS AND CONSULT YOUR DOCTOR. USING OTHER TOPICAL ACNE MEDICATION AT THE SAME TIME OR IMMEDIATELY FOLLOWING USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN.

DIRECTIONS

ALWAYS PATCH TEST A SMALL AREA BEFORE FIRST APPLICATION. APPLY SPARINGLY TO AFFECTED AREAS ONCE OR TWICE DAILY AS NEEDED, AVOIDING THE EYE AREA. DRYNESS AND LIGHT PEELING MAY OCCUR DURING THE FIRST FEW WEEKS OF USAGE.

INACTIVE INGREDIENTS

WATER, SULFUR 3%, BUTYLENE GLYCOL, CARBOMER, POTASSIUM SORBATE, PHENOXYETHANOL, SODIUM BENZOATE, SODIUM HYDROXIDE.

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

QUESTIONS OR COMMENTS:

WWW.CONTROLCORRECTIVE.COM

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MADE IN USA

01b UC_Clear Med 10pct

CLEAR MED   10%
benzoyl peroxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70764-107
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE10 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SULFUR (UNII: 70FD1KFU70)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70764-107-511 in 1 BOX06/09/2016
1NDC:70764-107-1174 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM00606/09/2016
Labeler - CONTROL CORRECTIVE SKINCARE INC (023999357)

Revised: 9/2023
Document Id: 05f61380-18b0-dc21-e063-6294a90adc73
Set id: 7acd1404-2af7-4ec4-b1e9-a905c9f823b8
Version: 7
Effective Time: 20230922
 
CONTROL CORRECTIVE SKINCARE INC