AMBI EVEN AND CLEAR EXFOLIATING WASH ACNE TREATMENT- salicylic acid gel

AMBI Even and Clear Exfoliating Wash Acne Treatment by

Drug Labeling and Warnings

AMBI Even and Clear Exfoliating Wash Acne Treatment by is a Otc medication manufactured, distributed, or labeled by AMBI ENTERPRISES, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Salicylic acid 1.5%

Purpose

Acne Treatment 

Use

for the treatment of acne

Warnings

For external use only

When using this product

skin irritation and dryness is 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.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

If pregnant or breast-feeding,

ask a health professional before use

Directions

• use every morning and evening
• wet area first
• apply a dime sized amount to palm and create a lather.
• gently massage over the face and neck
• rinse well 
• may also be used on chest and back
• because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
• if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Inactive ingredients

aqua (deionized water), disodium laureth sulfosuccinate, sodium cocoyl isetionate, cocamidopropyl betaine, sodium cocoyl taurate, polyacrylate-1 crosspolymer, sodium lauroamphoacetate, stearic acid, jojoba esters, salicylic acid, glycol stearate, zinc PCA, myristic acid, aminomethyl propanol avena sativa (oat) protein, sea whip extract, ethyl vanillin, dehydroacetic acid, benzyl alcohol.

Other information

store at 59°-86°F (15°-30°C)

Questions or comments

1-800-946-6354

Package Labeling:

INGREDIENTS AND APPEARANCE

AMBI EVEN AND CLEAR EXFOLIATING WASH ACNE TREATMENT 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73453-166
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	15 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCOL STEARATE (UNII: 0324G66D0E)
ZINC PIDOLATE (UNII: C32PQ86DH4)
MYRISTIC ACID (UNII: 0I3V7S25AW)
OAT (UNII: Z6J799EAJK)
PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5)
ETHYL VANILLIN (UNII: YC9ST449YJ)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
BENZYL ALCOHOL (UNII: LKG8494WBH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73453-166-05	141 g in 1 TUBE; Type 0: Not a Combination Product	07/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	07/13/2020

Labeler - AMBI ENTERPRISES, LLC (117015229)