WALGREENS ACNE CONTROL GEL- salicylic acid gel

Walgreens Acne Control Gel by

Drug Labeling and Warnings

Walgreens Acne Control Gel by is a Otc medication manufactured, distributed, or labeled by WALGREEN COMPANY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 2.0%

Purpose

Acne Treatment

Uses

• For the treatment of acne
• clears acne blemishes and allows skin to heal
• helps prevent new acne blemishes from forming

Warnings

For external use only

When using this product

• 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.
• avoid contact with eyes. If contact occurs, flush thoroughly with water.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• cleanse the skin thoroughly before applying this product.
• 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.

Other information

• may stain some fabrics

Inactive ingredients

behentrimonium methosulfate, carbomer, ceramide AP, ceramide EOP, ceramide NP, cetearyl alcohol, cetyl alcohol, chlorphenesin, cholesterol, disodium EDTA, glycerin, glycolic acid, guar hydroxypropyltrimonium chloride, lactic acid, niacinamide, phytosphingosine, sodium hyaluronate, sodium hydroxide, sodium lauroyl lactylate, water, xanthan gum

Label

INGREDIENTS AND APPEARANCE

WALGREENS ACNE CONTROL GEL 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0269
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
XANTHAN GUM (UNII: TTV12P4NEE)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
CHLORPHENESIN (UNII: I670DAL4SZ)
CHOLESTEROL (UNII: 97C5T2UQ7J)
GLYCOLIC ACID (UNII: 0WT12SX38S)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
LACTIC ACID (UNII: 33X04XA5AT)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CETYL ALCOHOL (UNII: 936JST6JCN)
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
NIACINAMIDE (UNII: 25X51I8RD4)
BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
CERAMIDE AP (UNII: F1X8L2B00J)
POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)
CERAMIDE NP (UNII: 4370DF050B)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0269-83	1 in 1 CARTON	05/02/2023
1		40 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	05/02/2023

Labeler - WALGREEN COMPANY (008965063)