DAILY ACNE CONTROL CLEANSER- benzoyl peroxide cream 
Topco Associates LLC

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.

----------

Top Care 264.005 264AI rev 1 - 264AJ

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

Adverse reactions

DISTRIBUTED BY

TOPCO ASSOCIATES LLC

ELK GROVE VILLAGE, IL 60007

TOPCO VIJ0422

QUESTIONS? 1-888-423-0139

topcare@topco.com

QUALITY GUARANTEED

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

*This product is not manufactured or distributed by the Johnson Consumer Products Company, 

distributor of Clean & Clear Continuous Control Acne Cleanser.

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 PEROXIDE104 mg  in 10 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)  
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 finalpart333D08/09/2022
Labeler - Topco Associates LLC (006935977)
Registrant - Vi-Jon, LLC (088520668)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(76162-264)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(76162-264)

Revised: 8/2022
Document Id: bf521f53-c3ea-40ec-8da9-70958f4627ec
Set id: 8474d917-7ee4-4d1d-8499-3520f771d2fd
Version: 1
Effective Time: 20220809
 
Topco Associates LLC