FDA.reportPublic FDA data

Ambi Even and Clear Foaming Cleanser

Manufacturer
L'Oreal USA Products Inc. | Product Quest Mfg, LLC
Effective date
2019-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:47:02

Label at a glance#

ProductAmbi Even and Clear Foaming Cleanser
Active ingredientSalicylic Acid
Label structure8 sections

Indications and uses

For the treatment of acne

Dosage and administration

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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 0.5%

Purpose

OTC - PURPOSE SECTION

Acne Medication

Uses

INDICATIONS & USAGE SECTION

  • For the treatment of acne

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

1-800-946-6354

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-06149967-061-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
Salicylic AcidO414PZ4LPZACTIB
Butylene Glycol3XUS85K0RAIACT
Citric Acid Monohydrate2968PHW8QPIACT
Cocamidopropyl Betaine5OCF3O11KXIACT
Edetate Disodium7FLD91C86KIACT
Disodium LauroamphodiacetateR4HKX6I64RIACT
GlycerinPDC6A3C0OXIACT
PEG-6 Caprylic/Capric GlyceridesGO50W2HWO8IACT
Polysorbate 207T1F30V5YHIACT
Sodium Ascorbyl Phosphate836SJG51DRIACT
Sodium BenzoateOJ245FE5EUIACT
Sodium C14-16 Olefin SulfonateO9W3D3YF5UIACT
.Alpha.-Tocopherol Acetate9E8X80D2L0IACT
Water059QF0KO0RIACT
Xanthan GumTTV12P4NEEIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
9a625499-1e87-40b2-bbf6-d31bf794c0e1f0de287e-482a-4232-a585-292bfd5335262019-12-31WarningsExact identifier
spl id: 9a625499-1e87-40b2-bbf6-d31bf794c0e1
spl set id: f0de287e-482a-4232-a585-292bfd533526

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.