CLN ACNE CLEANSER- salicylic acid 0.5% liquid liquid

CLN ACNE CLEANSER by

Drug Labeling and Warnings

CLN ACNE CLEANSER by is a Otc medication manufactured, distributed, or labeled by TopMD Skin Care, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Salicylic Acid 0.5%

Purpose

Acne Treatment

Uses

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.

Avoid contact with eyes.

If contact occurs, flush thoroughly with water

Keep out of reach of children.

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

Directions

Cleanse twice daily or as indicated by your physician. Treat whole area. Wet the skin. Dispense into wet hands. Massage area gently for 30 seconds working to create a lather. Rinse thoroughly with warm water. If bothersome dryness or peeling occurs, reduce use to once a day or every other day.

Inactive Ingredients

Purified Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Cocamide MEA, PEG-120 Methyl Glucose Trioleate, Propanediol, Sodium Hypochlorite, Disodium EDTA, Sodium Hydroxide.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CLN ACNE CLEANSER 
salicylic acid 0.5% liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69530-857
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
COCO MONOETHANOLAMIDE (UNII: C80684146D)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM HYPOCHLORITE (UNII: DY38VHM5OD)
WATER (UNII: 059QF0KO0R)
PROPANEDIOL (UNII: 5965N8W85T)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69530-857-46	100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/01/2016
2	NDC: 69530-857-47	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	09/01/2016

Labeler - TopMD Skin Care, Inc. (060946293)