WALGREENS APRICOT SCRUB ACNE TREATMENT- salicylic acid emulsion

WALGREENS APRICOT SCRUB ACNE TREATMENT by

Drug Labeling and Warnings

WALGREENS APRICOT SCRUB ACNE TREATMENT 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%

Purpose

Acne Treatment

Uses

for the treatment of acne.

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

• cover the entire affected area with a thin layer and rinse thoroughly 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
• store at room temperature

Inactive ingredients

water, juglans regia (walnut) shell powder, glyceryl stearate SE, propylene glycol, sodium laureth sulfate, zea mays (corn) kernel meal, cocamidopropyl betaine, cetearyl alcohol, triethanolamine, cetyl alcohol, PEG-100 stearate, glcyeryl stearate, cetyl acetate, ceteareth-20, polysorbate 60, carbomer, acetylated lanolin alcohol, fragrance (parfum), phenethyl alcohol, PPG-2-methyl ether, limonene, linalool, methylisothiazolinone, glycerin, prunus armeniaca (apricot) fruit extract, titanium dioxide (CI177891).

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALGREENS APRICOT SCRUB ACNE TREATMENT 
salicylic acid emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0951
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 g

Inactive Ingredients
Ingredient Name	Strength
JUGLANS REGIA SHELL (UNII: PJ10MT7VKA)
CORN GRAIN (UNII: C1Z9U7094Z)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
CETYL ACETATE (UNII: 4Q43814HXS)
ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)
POLYSORBATE 60 (UNII: CAL22UVI4M)
PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N)
APRICOT (UNII: 269CJD5GZ9)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
CETYL ALCOHOL (UNII: 936JST6JCN)
TROLAMINE (UNII: 9O3K93S3TK)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
LIMONENE, (+/-)- (UNII: 9MC3I34447)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0951-15	170 g in 1 TUBE; Type 0: Not a Combination Product	04/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	04/03/2020

Labeler - WALGREEN COMPANY (008965063)