MEDICATED PUMICE WASH- 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 CORRECTIVE - MEDICATED PUMICE WASH (70764-101)

ACTIVE INGREDIENTS

BENZOYL PEROXIDE (2.5%)

PURPOSE

ACNE TREATMENT

USE

A MEDICATED CLEANSING WASH THAT HELPS REDUCE ACNE BACTERIA AND OILY SKIN.

WARNINGS

AVOID THE EYE AREA. CONTAINS BENZOYL PEROXIDE. IF ANY IRRITATION OR DISCOMFORT OCCURS, DISCONTINUE USE AND CONTACT YOUR SKINCARE SPECIALIST. MAY BLEACH FABRIC. DO NOT USE ON CHILDREN UNDER 12 YEARS OF AGE.

DIRECTIONS

APPLY A SMALL AMOUNT TO PREMOISTENED SKIN AND LIGHTLY MASSAGE AFFECTED AREAS, THEN RINSE OFF. USE ONCE OR TWICE DAILY. REDUCE FREQUENCY IF SKIN GETS TOO DRY.

INACTIVE INGREDIENTS

WATER, JOJOBA ESTERS, AMMONIUM LAURYL SULFATE, PROPYLENE GLYCOL, CARBOMER, PHENOXYETHANOL, COCAMIDOPROPYL BETAINE, AMMONIUM XYLENESULFONATE, LAURYL ALCOHOL, SODIUM HYDROXIDE, MENTHA ARVENSIS LEAF OIL, ETHYLHEXYLGLYCERIN, SODIUM CHLORIDE, GLYCERIN, DIMETHICONE, POLYSORBATE 20.

KEEP OUT OF REACH OF CHILDREN.

QUESTIONS OR COMMENTS

WWW.CONTROLCORRECTIVE.COM

TOLL FREE 1-866-290-4290

MADE IN USA

01b UC_Medicated Pumice Wash

MEDICATED PUMICE WASH
benzoyl peroxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70764-101
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM)	BENZOYL PEROXIDE	2.5 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 40-44) (UNII: AS2SZ9757N)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM)
LAURYL ALCOHOL (UNII: 178A96NLP2)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHICONE (UNII: 92RU3N3Y1O)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:70764-101-56	1 in 1 BOX	06/07/2016	01/02/2021
1	NDC:70764-101-16	198 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	06/07/2016	01/02/2021

Labeler - CONTROL CORRECTIVE SKINCARE INC (023999357)

Name	Address	ID/FEI	Business Operations
Establishment
Chemolee Lab Corporation		809982754	manufacture(70764-101)

Revised: 9/2023

Document Id: 05f60b1c-0465-b259-e063-6294a90a7420

Set id: 25a5c1f0-65e2-4151-ab2c-a83a22095410

Version: 6

Effective Time: 20230922

CONTROL CORRECTIVE SKINCARE INC