ACNE AND OIL CONTROL- salicylic acid gel

ACNE AND OIL CONTROL by

Drug Labeling and Warnings

ACNE AND OIL CONTROL by is a Otc medication manufactured, distributed, or labeled by Skin Authority LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS:

SALICYLIC ACID 2%

PURPOSE

PURPOSE:

ACNE TREATMENT

INDICATIONS & USAGE

USES:

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

WARNINGS

WARNINGS:

FOR EXTERNAL USE ONLY.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

OTHER SAFETY INFORMATION

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

STOP USE

IF IRRITATION DEVELOPS, DISCONTINUE USE.

DOSAGE & ADMINISTRATION

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.

INACTIVE INGREDIENT

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

QUESTIONS? +1-760-268-0047

PRINCIPAL DISPLAY PANEL

SKIN AUTHORITY

ACNE AND OIL CONTROL

1.7 FL OZ / 50 ML

INGREDIENTS AND APPEARANCE

ACNE AND OIL CONTROL 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 46007-101
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: 46007-101-12	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/19/2012
2	NDC: 46007-101-11	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 final	part333D	04/19/2012

Labeler - Skin Authority LLC (136549396)

Registrant - Skin Authority LLC (136549396)