ACNE CLEANSER KISSABLE- salicylic acid solution

Acne Cleanser by

Drug Labeling and Warnings

Acne Cleanser by is a Otc medication manufactured, distributed, or labeled by BRANDS INTERNATIONAL, Brands International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient Purpose

Salicylic Acid 1% ............Acne Treatment

PURPOSE

for the treatment of Acne

INDICATIONS & USAGE

clears up acne blemishes, blackheads and whiteheads

penetrates pores to control acne blemishes

helps prevent new acne blemishs from forming

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Wet face

Squeeze product into hands

massage over entire face

rinse thoroughly

for optimal results use up to 2-3 times per week

WARNINGS

Warning: for external use only. skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time.

When using this product avoid contact with eyes. If contact occurs, flush thoroughly with water.

OTHER SAFETY INFORMATION

Store at room temparture

INACTIVE INGREDIENT

Inactive Ingredients:water, cocamidopropyl betaine, propylene glycol, sodium chloride, fragrance, Tetra sodium EDTA, aloe barbadensis leaf extract, methylchloroisothiazolinone, methylisothiazoline,

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ACNE CLEANSER  KISSABLE
salicylic acid solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50157-021
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	1 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
HYDROXYMETHYL CELLULOSE (UNII: 273FM27VK1)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE SODIUM (UNII: MP1J8420LU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50157-021-14	147 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/10/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	05/10/2024

Labeler - BRANDS INTERNATIONAL (243748238)

Establishment
Name	Address	ID/FEI	Business Operations
Brands International		243748238	manufacture(50157-021)