CLARIFYING PEEL- salicylic acid gel

CLARIFYING LIQUID PEEL by

Drug Labeling and Warnings

CLARIFYING LIQUID PEEL by is a Otc medication manufactured, distributed, or labeled by Skin Authority LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

SALICYLIC ACID 2%

PURPOSE

ACNE TREATMENT

USES

HELPS ELIMINATE ACNE-CAUSING BACTERIA, CALMS INFLAMMATION, AND MINIMIZES EXCESS OIL.

WARNINGS

FOR EXTERNAL USE ONLY.

AVOID CONTACT WITH EYES AND EYELIDS. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER.

IF IRRITATION DEVELOPS, DISCONTINUE USE.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

DIRECTIONS

APPLY WITH FINGERTIPS OR COTTON PAD IMMEDIATELY AFTER CLEANSING, COVERING FACE AND INFLAMED AREAS. CONTINUE WITH DAILY CARE ROUTINE. REAPPLY THROUGHOUT THE DAY TO REMOVE EXCESS OIL AND DIRT.

OTHER INGREDIENTS

WATER, GLYCOLIC ACID, HAMAMELIS VIRGINIANA (WITCH HAZEL) EXTRACT, SD ALCOHOL, SODIUM PCA, PPG-5-CETETH-20, SODIUM HYDROXIDE, ALOE BARBADENSIS LEAF JUICE, POLYSORBATE 80, PHENOXYETHANOL, CAPRYLYL GLYCOL, ETHYLHEXYLGLYCERIN, HEXYLENE GLYCOL, METHYLGLUCETH-20.

QUESTIONS?

+1-760-268-0047

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CLARIFYING PEEL 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 46007-102
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)
GLYCOLIC ACID (UNII: 0WT12SX38S)
HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
ALCOHOL (UNII: 3K9958V90M)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
PPG-5-CETETH-20 (UNII: 4AAN25P8P4)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 46007-102-12	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/19/2012
2	NDC: 46007-102-11	20 mL in 1 TUBE; Type 0: Not a Combination Product	04/19/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	04/19/2012

Labeler - Skin Authority LLC (136549396)