FOAMING CLEANSER- salicylic acid liquid

Foaming Cleanser by

Drug Labeling and Warnings

Foaming Cleanser by is a Otc medication manufactured, distributed, or labeled by Allure Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient:

Salicylic Acid 2%

PURPOSE

Purpose: Acne Treatment

INDICATIONS & USAGE

Uses: For the treatment of acne

Gently cleanses and maintains optimal moisture balance.

For all skin types

WARNINGS

Warning: For external use only

DO NOT USE

If excessive dryness or peeling occurs

WHEN USING

Avoid eye area

STOP USE

If excessive dryness or peeling occurs

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Direction:

Use daily. Thoroughly lather foam over wet skin, rinse well and pat dry. Avoid eye area. If excessive dryness or peeling occurs, reduce application to every other day.

OTHER SAFETY INFORMATION

Using other topical acne medication 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.

INACTIVE INGREDIENT

Inactive Ingredient:

Water (Aqua), Alkyl (C10-16) Ether Sulfate Sodium Salt, Cocamidopropyl Betaine, Butylene Glycol, Hydrolyzed Wheat Protein, Alcohol (C12-15 Ln. saturated), Ethoxylate, Hydrolyzed Wheat Starch, Caprylyl Glycol, Phenoxyethanol, Aloe Barbadensis Leaf Extract, Rosmarinus Officinalis ( Rosemary) Leaf Extract, Sodium Hydroxide, Ethylhexyl Glycerin, Hexylene Glycol, Sodium Chloride, Lavandula Angustifolia ( Lavender) Leaf Oil O.E., Glycerin.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FOAMING CLEANSER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4239
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
C12-15 ALCOHOLS (UNII: 2C8M6XLB5C)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
1-ETHOXYUNDECANE (UNII: R428J6A8Q2)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ROSEMARY (UNII: IJ67X351P9)
(C10-C16)ALKYLDIMETHYLAMINE OXIDE (UNII: LF6BKC321J)
STARCH, WHEAT (UNII: 79QS2MG2LP)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA LEAF (UNII: XY6Z280JTM)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4239-1	50 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/07/2023
2	NDC: 62742-4239-2	125 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/07/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	12/07/2023

Labeler - Allure Labs (926831603)

Registrant - Allure Labs (926831603)

Establishment
Name	Address	ID/FEI	Business Operations
Allure Labs		926831603	manufacture(62742-4239)