AMBI EVEN AND CLEAR FOAMING CLEANSER- salicylic acid liquid 
L'Oreal USA Products Inc.

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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Drug Facts

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

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AMBI EVEN AND CLEAR FOAMING CLEANSER 
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-061
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-061-01177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/06/201708/24/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D06/15/201408/24/2020
Labeler - L'Oreal USA Products Inc. (002136794)
Establishment
NameAddressID/FEIBusiness Operations
Product Quest Mfg, LLC927768135MANUFACTURE(49967-061)

Revised: 12/2019
Document Id: 9a625499-1e87-40b2-bbf6-d31bf794c0e1
Set id: f0de287e-482a-4232-a585-292bfd533526
Version: 2
Effective Time: 20191231
 
L'Oreal USA Products Inc.