TOPICALS CLEARLY MIST- salicylic acid liquid

Topicals Clearly Mist by

Drug Labeling and Warnings

Topicals Clearly Mist by is a Otc medication manufactured, distributed, or labeled by Topiderm, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredient

Salicylic acid 2%

Purpose

Acne treatment

Use

For the treatment of acne

Warnings

For external use only.

When using this product, keep away from face. If contact occurs, flush thoroughly with water.

If irritation occurs when using two acne topical medications, only use one topical acne medication at a time.

Do not inhale.

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

Directions

Spray a thin layer onto clean skin 1-3 times daily. Allow product to sink in for 30-60 seconds and do not rub in. If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Other information

Do not store at temperatures above 120°F.

Questions?

+1-323-776-1963

Inactive ingredients

Water/Aqua/Eau, Alcohol Denat., Hypochlorous Acid, Glycolic Acid, Allantoin, Zinc PCA, Potassium Hydroxide, Sodium Benzoate

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Dist. by Topicals
Santa Monica, CA 90405

PRINCIPAL DISPLAY PANEL - 100 ml Bottle Carton

CLEARLY

TOPICALS

Clarifying & Calming Mist

For acne-prone skin

100 ml / 3.4 fl oz

INGREDIENTS AND APPEARANCE

TOPICALS CLEARLY MIST 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51326-307
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
HYPOCHLOROUS ACID (UNII: 712K4CDC10)
GLYCOLIC ACID (UNII: 0WT12SX38S)
ALLANTOIN (UNII: 344S277G0Z)
ZINC PIDOLATE (UNII: C32PQ86DH4)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51326-307-01	1 in 1 BOX	09/20/2024
1		100 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH DRUG	M006	09/20/2024

Labeler - Topiderm, Inc. (049121643)

Registrant - Topiderm, Inc. (049121643)

Establishment
Name	Address	ID/FEI	Business Operations
Topiderm, Inc.		049121643	MANUFACTURE(51326-307)