SALICYLIC WASH- salicylic acid lotion

SALICYLIC WASH by

Drug Labeling and Warnings

SALICYLIC WASH by is a Otc medication manufactured, distributed, or labeled by CONTROL CORRECTIVE SKINCARE INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

SALICYLIC ACID (2.0%)

PURPOSE

ACNE TREATMENT

USE

THIS GENTLE FOAMING CLEANSER WORKS TO SMOOTH AND EXFOLIATE DEAD SKIN BUILDUP. MAY BE USED DAILY OR AS DIRECTED BY YOUR SKINCARE SPECIALIST.

WARNINGS

AVOID EYE AREA. DISCONTINUE USE IF IRRITATION OCCURS. DO NOT USE IF ALLERGIC TO ASPERIN.

DIRECTIONS

APPLY A SMALL AMOUNT TO PRE-MOISTENED FINGERS AND LIGHTLY MASSAGE TO AFFECTED AREAS. RINSE WITH TEPID WATER. MAY BE USED ONCE OR TWICE DAILY DEPENDING ON SKIN TYPE.

INACTIVE INGREDIENTS

WATER, AMMONIUM LAURETH SULFATE, AMMONIUM LAURYL SULFATE, COCAMIDOPROPYL BETAINE, ALOE BARBADENSIS LEAF JUICE, GLYCOL STEARATE, SODIUM COCOYL ISETHIONATE, SODIUM LAUROAMPHOACETATE, PHENOXYETHANOL, CHAMOMILE RECUTITA (MATRICARIA) FLOWER EXTRACT, METHYLISOTHIAZOLINONE.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

QUESTIONS OR COMMENTS

WWW.CONTROLCORRECTIVE.COM

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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SALICYLIC WASH 
salicylic acid lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70764-102
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)
AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCOL STEARATE (UNII: 0324G66D0E)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CHAMOMILE (UNII: FGL3685T2X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70764-102-56	1 in 1 BOX	06/09/2016
1	NDC: 70764-102-16	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	06/09/2016

Labeler - CONTROL CORRECTIVE SKINCARE INC (023999357)