ACNE TREATMENT- benzoyl peroxide gel 
Walgreens Co.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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10% Benzoyl Peroxide Acne Medicated Gel
229.001/229AC-AD

Active ingredient

Benzoyl peroxide 10%

Purpose

Acne medication

Use

for the treatment of acne

Warnings

For external use only

Do not use if you

When using this product

Stop use and ask a doctor if

irritation becomes severe

Keep out of reach of children

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

Directions

Inactive ingredients

carbomer, disodium EDTA, hydroxypropyl methylcellulose, laureth-4, sodium hydroxide, water

This acne medication contains maximum strength benzoyl peroxide.  The micronized benzoyl peroxide formula goes to work immediately, releasing the medicine deep into the pore where pimples begin.

*Walgreens pharmacist survey

**This product is not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of Clean & Clear Persa-Gel 10.

Distributed by Walgreen Co., 200 Wilmot Rd., Deerfield, IL 600015

walgreens.com (c) 2017 Walgreen Co.

princpal display panel

*Walgreens pharmacist recommended

Maximum Strength Acne Treatment Gel

10% benzoyl peroxide/acne medication

NET WT 1 OZ (28 g)

image description

ACNE TREATMENT 
benzoyl peroxide gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0229
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
LAURETH-4 (UNII: 6HQ855798J)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0229-101 in 1 PACKAGE12/02/2011
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D12/02/2011
Labeler - Walgreens Co. (008965063)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(0363-0229)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(0363-0229)
Establishment
NameAddressID/FEIBusiness Operations
Remar117825116pack(0363-0229)

Revised: 9/2022
Document Id: c837c445-209c-40bb-82e1-efa8c2966855
Set id: 07721aa6-867a-436f-8c88-ab135f02a6b5
Version: 21
Effective Time: 20220906
 
Walgreens Co.