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NDC 00363-0951-15 WALGREENS APRICOT SCRUB ACNE TREATMENT 20 mg/g Details

WALGREENS APRICOT SCRUB ACNE TREATMENT 20 mg/g

WALGREENS APRICOT SCRUB ACNE TREATMENT is a TOPICAL EMULSION in the HUMAN OTC DRUG category. It is labeled and distributed by WALGREEN COMPANY. The primary component is SALICYLIC ACID.

MedlinePlus Drug Summary

Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions that involve scaling or overgrowth of skin cells such as psoriasis (a skin disease in which red, scaly patches form on some areas of the body), ichthyoses (inborn conditions that cause skin dryness and scaling), dandruff, corns, calluses, and warts on the hands or feet. Topical salicylic acid should not be used to treat genital warts, warts on the face, warts with hair growing from them, warts in the nose or mouth, moles, or birthmarks. Salicylic acid is in a class of medications called keratolytic agents. Topical salicylic acid treats acne by reducing swelling and redness and unplugging blocked skin pores to allow pimples to shrink. It treats other skin conditions by softening and loosening dry, scaly, or thickened skin so that it falls off or can be removed easily.

Related Packages: 00363-0951-15
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Salicylic Acid Topical

Product Information

NDC	00363-0951
Product ID	0363-0951_c68caf17-6add-5ce2-e053-2995a90a5655
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	WALGREENS APRICOT SCRUB ACNE TREATMENT
Proprietary Name Suffix	n/a
Non-Proprietary Name	SALICYLIC ACID
Product Type	HUMAN OTC DRUG
Dosage Form	EMULSION
Route	TOPICAL
Active Ingredient Strength	20
Active Ingredient Units	mg/g
Substance Name	SALICYLIC ACID
Labeler Name	WALGREEN COMPANY
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part333D
Listing Certified Through	2024-12-31

Package

Package Images

NDC 00363-0951-15 (00363095115)

Pricing Information	N/A
NDC Package Code	0363-0951-15
Billing NDC	00363095115
Package	170 g in 1 TUBE (0363-0951-15)
Marketing Start Date	2020-04-03
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL c0081097-424c-4ebf-ae9e-750650e67e69 Details

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

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

Ingredient Name	Strength
Inactive Ingredients
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)

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

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	04/03/2020

Labeler - WALGREEN COMPANY (008965063)

Revised: 7/2021

Document Id: c68caf17-6add-5ce2-e053-2995a90a5655

Set id: c0081097-424c-4ebf-ae9e-750650e67e69

Version: 3

Effective Time: 20210707