AMBI EVEN AND CLEAR FOAMING CLEANSER- salicylic acid liquid

Ambi Even and Clear Foaming Cleanser by

Drug Labeling and Warnings

Ambi Even and Clear Foaming Cleanser by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc., Product Quest Mfg, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic Acid 0.5%

Purpose

Acne Medication

Uses

• For the treatment of acne

Warnings

For external use only.

When using this product and other topical acne medications at the same time or immediately following use of the product, dryness or irritation of the skin may be increased. If this occurs, only one medication should be used unless directed by a doctor. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

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

Directions

• Moisten face and pump cleanser into your hand or cloth.
• Massage lather over face.
• Rinse thoroughly and pat dry
• If you experience dryness or irritation, use less frequently.

Inactive ingredients

Butylene Glycol, Citric Acid, Cocamidopropyl Betaine, Disodium EDTA, Disodium Lauroamphodiacetate, Fragrance, Glycerin, Glycine Soja (Soybean) Protein, PEG-16 Macadamia Glycerides, PEG-16 Soy Sterol, PEG-6 Caprylic/Capric Glycerides, Polysorbate 20, Sodium Ascorbyl Phosphate, Sodium Benzoate, Sodium C14-16 Olefin Sulfonate, Tocopheryl Acetate, Water, Xanthan Gum

Questions/Comments?

1-800-946-6354

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AMBI EVEN AND CLEAR FOAMING CLEANSER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-061
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Butylene Glycol (UNII: 3XUS85K0RA)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Edetate Disodium (UNII: 7FLD91C86K)
Disodium Lauroamphodiacetate (UNII: R4HKX6I64R)
Glycerin (UNII: PDC6A3C0OX)
PEG-6 Caprylic/Capric Glycerides (UNII: GO50W2HWO8)
Polysorbate 20 (UNII: 7T1F30V5YH)
Sodium Ascorbyl Phosphate (UNII: 836SJG51DR)
Sodium Benzoate (UNII: OJ245FE5EU)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Water (UNII: 059QF0KO0R)
Xanthan Gum (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-061-01	177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/06/2017	08/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	06/15/2014	08/24/2020

Labeler - L'Oreal USA Products Inc. (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg, LLC		927768135	MANUFACTURE(49967-061)