DAILY ACNE CONTROL CLEANSER- benzoyl peroxide cream 
Topco Associates LLC

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Top Care 264.005/264AJ
Acne Control Cleanser

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. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

Directions

Other information

Inactive ingredients

water, cetyl alcohol, petrolatum, acrylates/C10-30 alkyl acrylate crosspolymer, zinc lactate, steareth-2, glycerin, potassium cetyl phosphate, xanthan gum, benzyl alcohol, fragrance, disodium EDTA, laureth-4, BHT, sodium hydroxide, lactic acid, menthol

Disclaimer

*This product is not manufactured or distributed by the Johnson Consumer Products Company, distributor of Clean & Clear Continuous Control Acne Cleanser.

Adverse reactions

DISTRIBUTED BY

TOPCO ASSOCIATES LLC

ELK GROVE VILLAGE, IL 60007

TOPCO VIJA0422

QUESTIONS? 1-888-423-0139

topcare@topco.com

www.topcarebrand.com

QUALITY GUARANTEED

Scan here for more information or call 1-888-423-0139

principal display panel

TopCare ®beauty

DAILY ANCE CONTROL CLEANSER

10% Benzoyl Peroxide Acne Medication

Compare to CLEAN & CLEAR ®*

Keeps fighting acne even after you wash

PARABEN FREE

NET WT 5 OZ (141 g)

image description

DAILY ACNE CONTROL CLEANSER 
benzoyl peroxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76162-264
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE100 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
PETROLATUM (UNII: 4T6H12BN9U)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
ZINC LACTATE (UNII: 2GXR25858Y)  
STEARETH-2 (UNII: V56DFE46J5)  
GLYCERIN (UNII: PDC6A3C0OX)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
XANTHAN GUM (UNII: TTV12P4NEE)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
LAURETH-4 (UNII: 6HQ855798J)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
MENTHOL (UNII: L7T10EIP3A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76162-264-28141 g in 1 TUBE; Type 0: Not a Combination Product08/09/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00608/09/2022
Labeler - Topco Associates LLC (006935977)
Registrant - Nice-Pak Products, LLC (119091520)
Establishment
NameAddressID/FEIBusiness Operations
Nice-Pak Products, LLC119091514manufacture(76162-264)

Revised: 2/2026
Document Id: 4ab83e23-0910-ca30-e063-6394a90a6eac
Set id: 8474d917-7ee4-4d1d-8499-3520f771d2fd
Version: 5
Effective Time: 20260213
 
Topco Associates LLC