SO TOTALLY CLEAN DEEP PORE CLEANSER- salicylic acid liquid

SO TOTALLY CLEAN DEEP PORE CLEANSER by

Drug Labeling and Warnings

SO TOTALLY CLEAN DEEP PORE CLEANSER by is a Otc medication manufactured, distributed, or labeled by ASPIRE BRANDS INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

SALICYLIC ACID 0.5%

PURPOSE

ACNE TREATMENT

USE

ACNE TREATMENT TO HELP CLEAR UP AND PREVENT NEW ACNE BLEMISHES, BLACKHEADS, AND WHITEHEADS.

WARNINGS

• FOR EXTERNAL USE ONLY.
• FLAMMABLE - KEEP AWAY FROM OPEN FIRE OR FLAME.

WHEN USING

WHEN USING THIS PRODUCT

• AVOID CONTACT WITH EYES. IF CONTACT OCCURS, FLUSH THOROUGHLU WITH WATER.
• SKIN IRRITATION AND DRYNESS IS MORE LIKELY TO OCCUR IF YOU USE ANOTHER TOPICAL ACNE MEDICATION AT THE SAME TIME. IF IRRITATION OCCURS, ONLY USE ONE TOPICAL ACNE MEDICATION AT A TIME.

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

• CLEAN THE SKIN THOROUGHLY BEFORE APPLYING THIS PRODUCT.
• MOISTEN A COTTON BALL. COVER THE ENTIRE AFFECTED AREA WITH A THIN LAYER ONE TO THREE TIMES DAILY.
• BECAUSE EXCESSIVE DRYING OF THE SKIN MAY OCCUR, START WITH ONE APPLICATION DAILY, THEN GRADUALLY INCREASE TO TWO OR THREE TIMES DAILY IF NEEDED OR AS DIRECTED BY A DOCTOR.
• IF BOTHERSOME DRYNESS OR PEELING OCCURS, REDUCE APPLICATION TO ONCE A DAY OR EVERY OTHER DAY.

INACTIVE INGREDIENTS

ALCOHOL DENAT., WATER, SODIUM PCA, LACTIC ACID, FRAGRANCE, ALLANTOIN, SODIUM CARBONATE, RED 4, YELLOW 5, YELLOW 6.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SO TOTALLY CLEAN DEEP PORE CLEANSER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70626-104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
LACTIC ACID (UNII: 33X04XA5AT)
ALLANTOIN (UNII: 344S277G0Z)
SODIUM CARBONATE (UNII: 45P3261C7T)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70626-104-21	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/02/2016
2	NDC: 70626-104-22	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/17/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	05/02/2016

Labeler - ASPIRE BRANDS INC (832462811)