ACNE SPOT TREATMENT- salicylic acid gel
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 (70764-105)

ACTIVE INGREDIENTS

SALICYLIC ACID (2.0%)

PURPOSE

ACNE TREATMENT

USE

AN EXFOLIATING GEL THAT AIDS IN REDUCING ACNE BREAKOUTS.

WARNINGS

FOR EXTERNAL USE ONLY. DO NOT USE ON BROKEN SKIN. AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.

DIRECTIONS

APPLY A SMALL AMOUNT WITH FINGERS TO CLEAN, DRY SKIN. MAY BE USED ALL OVER THE AFFECTED AREA OR USED TO SPOT TREAT BLEMISHES. IF ANY DISCOMFORT OCCURS, REDUCE FREQUENCY OR DISCONTINUE USE.

INACTIVE INGREDIENTS

WATER, GLYCOLIC ACID (3%), SD ALCOHOL 40-A, ALOE BARBADENSIS LEAF JUICE, WITCH HAZEL, GLYCERIN, TRIETHANOLAMINE, METHYL GLUCETH-20, SODIUM LACTATE, FRUCTOSE, UREA, NIACINAMIDE, INOSITOL, SODIUM BENZOATE, LACTIC ACID, HYDROXYETHYLCELLULOSE, PHENOXYETHANOL, PANTHENOL, ALLANTOIN, GLUCOSAMINE SULFATE, METHYLISOTHIAZOLINONE.

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

DO NOT USE IF ALLERGIC TO ASPERIN.

QUESTIONS OR COMMENTS:

WWW.CONTROLCORRECTIVE.COM

TOLL FREE 1-866-290-4290

MADE IN USA

01b UC_Acne Spot Treatment

ACNE SPOT TREATMENT
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70764-105
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCOLIC ACID (UNII: 0WT12SX38S)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WITCH HAZEL (UNII: 101I4J0U34)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
SODIUM LACTATE (UNII: TU7HW0W0QT)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
FRUCTOSE (UNII: 6YSS42VSEV)
UREA (UNII: 8W8T17847W)
NIACINAMIDE (UNII: 25X51I8RD4)
INOSITOL (UNII: 4L6452S749)
SODIUM BENZOATE (UNII: OJ245FE5EU)
LACTIC ACID (UNII: 33X04XA5AT)
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PANTHENOL (UNII: WV9CM0O67Z)
ALLANTOIN (UNII: 344S277G0Z)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70764-105-51	1 in 1 BOX	06/09/2016
1	NDC:70764-105-11	30 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	06/09/2016

Labeler - CONTROL CORRECTIVE SKINCARE INC (023999357)