CREAMY ACNE FACE WASH- benzoyl peroxide 4% cream 
CVS

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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CVS Health

Drug Facts

Active ingredient                               Purpose
Benzoyl Peroxide 4%.........................Acne Treatment

Use For the treatment of acne.

Warnings
For external use only.
Do not use if you have very sensitive skin or if you
are sensitive to benzoyl peroxide.
When using this product • skin irritation and
dryness are 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. • rinse right away with water if it gets in eyes
• avoid unnecessary sun exposure and use a sunscreen
• avoid contact with the eyes, lips, and mouth • avoid
contact with hair and dyed fabrics, which may be
bleached by this product • skin irritation may occur,
characterized by redness, burning, itching, peeling, or
possibly swelling. Irritation may be reduced by using
the product less frequently or in a lower concentration.
Stop use and consult a doctor if • irritation becomes severe.

Directions • Wet face • Apply to hands and work
into a lather • Massage face gently • Rinse thoroughly
and pat dry • Cleanse twice a day • If going outside,
apply sunscreen after using this product. If irritation or
sensitivity develops, stop use of both products and
consult a doctor.

Inactive ingredients
Water, Sodium Cocoyl Isethionate, Cetearyl Alcohol,
Cocamidopropyl Betaine, Potassium Lauryl Phosphate,
Glycerin, Disodium Laureth Sulfosuccinate, Sodium
Hydroxide, Glycolic Acid, Mineral Oil, Lactic Acid, Titanium
Dioxide, Acrylates/C10-30 Alkyl Acrylate Crosspolymer,
Sodium PCA, Dimethyl Isosorbide, Sodium Lauryl
Sulfoacetate, Phenoxyethanol, Ethylhexylglycerin.

image descriptionimage description

CREAMY ACNE FACE WASH 
benzoyl peroxide 4% cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-444
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzoyl Peroxide (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) Benzoyl Peroxide4 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
Dimethyl Isosorbide (UNII: SA6A6V432S)  
Disodium Laureth Sulfosuccinate (UNII: D6DH1DTN7E)  
Ethylhexylglycerin (UNII: 147D247K3P)  
Glycerin (UNII: PDC6A3C0OX)  
Glycolic Acid (UNII: 0WT12SX38S)  
Lactic Acid (UNII: 33X04XA5AT)  
Mineral Oil (UNII: T5L8T28FGP)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
Potassium Lauryl Phosphate (UNII: C4QT53N4MK)  
Sodium Cocoyl Isethionate (UNII: 518XTE8493)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Sodium Lauryl Sulfoacetate (UNII: D0Y70F2B9J)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
Titanium Dioxide (UNII: 15FIX9V2JP)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-444-05204 g in 1 TUBE; Type 0: Not a Combination Product06/20/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D06/20/2018
Labeler - CVS (062312574)
Registrant - Product Quest Mdf (927768135)
Establishment
NameAddressID/FEIBusiness Operations
Product Quest Mdf927768135manufacture(69842-444) , label(69842-444)

Revised: 4/2018
Document Id: cda53cd8-2754-4cfa-8c2e-c3613a0b1afd
Set id: 9cb15858-7a2b-44ef-a8f0-c890c55f47df
Version: 1
Effective Time: 20180423
 
CVS