Skin Authority - ACNE AND OIL CONTROL GEL (46007-101) - DELIST

ACTIVE INGREDIENTS:

SALICYLIC ACID 2%

PURPOSE:

ACNE TREATMENT

USES:

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

WARNINGS:

FOR EXTERNAL USE ONLY.

KEEP OUT OF REACH OF CHILDREN.

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

IF IRRITATION DEVELOPS, DISCONTINUE USE.

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.

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

SKIN AUTHORITY

ACNE AND OIL CONTROL

1.7 FL OZ / 50 ML

51101(revE)50ml-AcneOilControl

ACNE AND OIL CONTROL
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:46007-101
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)
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:46007-101-12	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/19/2012	05/09/2022
2	NDC:46007-101-11	20 mL in 1 TUBE; Type 0: Not a Combination Product	04/19/2012	05/09/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	04/19/2012	05/09/2022

Labeler - Skin Authority LLC (136549396)

Revised: 10/2023

Document Id: 06fe49cf-6c7a-81d9-e063-6294a90a6af2

Set id: 8ae86330-28f0-4d22-914e-be7963993f12

Version: 9

Effective Time: 20231005

Skin Authority LLC