MEDICATED PUMICE WASH- benzoyl peroxide lotion

MEDICATED PUMICE WASH by

Drug Labeling and Warnings

MEDICATED PUMICE WASH by is a Otc medication manufactured, distributed, or labeled by CONTROL CORRECTIVE SKINCARE INC, Chemolee Lab Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

KEEP OUT OF REACH OF CHILDREN.

QUESTIONS OR COMMENTS

WWW.CONTROLCORRECTIVE.COM

TOLL FREE 1-866-290-4290

MADE IN USA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MEDICATED PUMICE WASH 
benzoyl peroxide lotion

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

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

Inactive Ingredients
Ingredient Name	Strength
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)

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

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

Labeler - CONTROL CORRECTIVE SKINCARE INC (023999357)

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