CRMY ACNE WASH CVS- benzoyl peroxide 4.00% cream

CRMY ACNE WASH by

Drug Labeling and Warnings

CRMY ACNE WASH by is a Otc medication manufactured, distributed, or labeled by CVS, Product Quest Mfg, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient                       Purpose

Benzoyl Peroxide – 4.00%          Acne Treatment

PURPOSE

INDICATIONS & USAGE

​Uses​ for treatment of acne

WarningsFor 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 is 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 eyes, lips, and mouth avoid contact with hair and dyed fabrics, which may be bleached by this product skin irritation may occurs, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.

Keep out of reach of the children
If product is swallowed, get medical help or contact a Poison Control Center right away

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

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Cetearyl Alcohol, Cocamidopropyl Betaine, Glycerin, Glycolic Acid, Dimethyl Isosorbide, Imidazolidinyl Urea, Lactic Acid, Methylparaben, Mineral Oil, Potassium Lauryl Sulfate, Purified Water, Sodium Cocoyl Isethionate, Sodium , Hydroxide, Sodium Lauryl Sulfate, Sodium PCA, Titanium Dioxide

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CRMY ACNE WASH  CVS
benzoyl peroxide 4.00% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-031
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM)	BENZOYL PEROXIDE	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCOLIC ACID (UNII: 0WT12SX38S)
DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)
IMIDUREA (UNII: M629807ATL)
LACTIC ACID (UNII: 33X04XA5AT)
METHYLPARABEN (UNII: A2I8C7HI9T)
MINERAL OIL (UNII: T5L8T28FGP)
POTASSIUM LAURYL SULFATE (UNII: PS6855FO7F)
WATER (UNII: 059QF0KO0R)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-031-05	1 in 1 CARTON	11/26/2014
1		204 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	11/26/2014

Labeler - CVS (062312574)

Registrant - Product Quest Mfg, LLC (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg, LLC		927768135	manufacture(69842-031) , label(69842-031)