DAILY CARE FOAMING CLEANSER ACNE TREATMENT- salicylic acid liquid

DAILY CARE FOAMING CLEANSER by

Drug Labeling and Warnings

DAILY CARE FOAMING CLEANSER by is a Otc medication manufactured, distributed, or labeled by OMP, INC., G.S. COSMECEUTICAL USA, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Acne treatment gel

Uses

• for the treatment of acne
• dries up acne pimples
• helps prevent new acne pimples

Warnings

For external use only

When using this product

• using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

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.

Directions

• use AM and PM
• wet face
• gently massage product all over face for 20-30 seconds avoiding eye area
• rinse thoroughly and pat dry
• wait 10-15 minutes to allow skin to dry completely

Other information

• store away from heat and direct sunlight
• store at controlled room temperature: 15°C–25°C (59°F–77°F)

Inactive ingredients

butyl avocadate, cetyl hydroxyethylcellulose, cocamidopropyl betaine, disodium EDTA, ethoxydiglycol, Ext. Violet 2 (CI 60730), fragrance, menthol, menthyl lactate, sodium laureth sulfate, sodium lauryl sulfate, water (aqua)

Questions or comments?

1.800.636.7546

Monday–Friday 9 a.m.–4 p.m. Pacific Time

SPL UNCLASSIFIED SECTION

Distributed by OMP, Inc., Long Beach, CA 90806

PRINCIPAL DISPLAY PANEL - 1 L Bottle Label

FOR PROFESSIONAL USE ONLY

OBAGI®
MEDICAL

Daily Care
Foaming Cleanser

Salicylic Acid 2%
Acne Treatment

Removes dirt and excess oil,
leaving skin clean and refreshed

33.8 fl. oz. (1 L)

INGREDIENTS AND APPEARANCE

DAILY CARE FOAMING CLEANSER   ACNE TREATMENT
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62032-129
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)
EDETATE DISODIUM (UNII: 7FLD91C86K)
MENTHOL (UNII: L7T10EIP3A)
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)

Product Characteristics
Color	PURPLE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62032-129-07	1000 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	01/18/2013

Labeler - OMP, INC. (790553353)

Establishment
Name	Address	ID/FEI	Business Operations
G.S. COSMECEUTICAL USA, INC.		017014734	MANUFACTURE(62032-129)