DAILY ACNE CONTROL CLEANSER- benzoyl peroxide cream 
Kroger Inc

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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Krogers 264.005-264AI rev 1

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

Questions?

1-800-632-6900

Disclaimer

CLEAN & CLEAR CONTINUOUS CONTROL are registered trademarks of Johnson & Johnson, New Brunswick, New Jersey 08933.  Johnson & Johnson is not affiliated with The Kroger Co. or this product.

Adverse Reactions Section

Quailty Guarantee 800.632.6900  www.kroger.com

Distributed by the Kroger Co., Cincinnati, Ohio 45202

264.005/264AI rev1

principal display panel

Compare to CLEAN & CLEAR

CONTINUOUS CONTROL

Acne Cleanser

care

CLARIFY

Let's be CLEAR

Daily Acne Control Cleanser

10% Benzoyl Peroxide Acne Medication

Keeps Fighting Acne After You Wash

Kroger

NET WT 5 oz (141 g)

image description

DAILY ACNE CONTROL CLEANSER 
benzoyl peroxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-264
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)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
LACTIC ACID (UNII: 33X04XA5AT)  
MENTHOL (UNII: L7T10EIP3A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30142-264-56141 g in 1 TUBE; Type 0: Not a Combination Product08/18/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D08/18/2014
Labeler - Kroger Inc (006999528)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(30142-264)

Revised: 3/2021
Document Id: d1114976-e059-4443-911f-db50cf94e510
Set id: 2f1552b7-2f83-447d-b8ec-ee8d20fe8083
Version: 10
Effective Time: 20210312
 
Kroger Inc