ACNE WASH KISSABLE- salicylic acid gel

Acne Wash by

Drug Labeling and Warnings

Acne Wash 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 2% ............Acne Treatment

PURPOSE

for the treatment of Acne

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.

INDICATIONS & USAGE

For treatment of acne

DOSAGE & ADMINISTRATION

Clean twice a day

Wet face, apply to hands add water and work into a lather

Massage fae gently

Rinse thoroughly

WARNINGS

Warning: for external use only.

Ask a doctor or pharmacist before use if you are using other topical acne medications at the same time or immediately following use of this product. This may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

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 WASH  KISSABLE
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50157-012
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 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)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50157-012-20	206 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/27/2023
2	NDC: 50157-012-23	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/27/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	02/27/2023

Labeler - BRANDS INTERNATIONAL (243748238)

Establishment
Name	Address	ID/FEI	Business Operations
Brands International		243748238	manufacture(50157-012)