ADVANCED 3 IN 1 EXFOLIATING CLEANSER- benzoyl peroxide 5.0% cream

Advanced 3 in 1 Exfoliating Cleanser by

Drug Labeling and Warnings

Advanced 3 in 1 Exfoliating Cleanser by is a Otc medication manufactured, distributed, or labeled by CVS, Product Quest Mfg.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                                  Purpose
Benzoyl Peroxide 5%.............................................Acne Treatment

PURPOSE

INDICATIONS & USAGE

Use For the 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 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 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.

DOSAGE & ADMINISTRATION

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 INGREDIENT

Inactive ingredients

Water,
Polyacrylamide, C13-14 Isoparaffin,
Cocamidopropyl Betaine, Jojoba Esters,
Laureth-7, Phenoxyethanol,
Ethylhexylglycerin.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ADVANCED 3 IN 1 EXFOLIATING CLEANSER 
benzoyl peroxide 5.0% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-839
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM)	BENZOYL PEROXIDE	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
C13-14 Isoparaffin (UNII: E4F12ROE70)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Laureth-7 (UNII: Z95S6G8201)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ethylhexylglycerin (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-839-04	148 mL in 1 TUBE; Type 0: Not a Combination Product	06/15/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	06/15/2017

Labeler - CVS (062312574)

Registrant - Product Quest Mfg. (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg.		927768135	manufacture(69842-839) , label(69842-839)