ZOONO SKIN CLEAR ACNE MEDICATION- acne medication - salicylic acid liquid

Zoono Skin Clear Acne Medication by

Drug Labeling and Warnings

Zoono Skin Clear Acne Medication by is a Otc medication manufactured, distributed, or labeled by Zoono USA, LLC, Holly Oak Chemical, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Ingredients Purpose

Salicylic Acid 0.5% Acne Medication

Uses

For treatment of acne.

Purpose

Acne Medication

Warnings

For external use only.

Do not use in the eyes.

Using other topical acne medications 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.

Stop use and ask a doctor if irritation and redness develop.

Keep out of reach of children.

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

Directions:

Cleanse the skin thoroughly before applying the medication. Cover the entire affected area with a thin layer one to three times daily. Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor. If dryness or peeling occurs, reduce application to one a day or every other day.

Inactive ingredients:

Ethyl alcohol, fragrance, trimethoxysilyl propyl dimethyl octadecyl ammonium chloride, water

Questions?

Telephone 1-844-966-6687

Monday through Friday

8:00am till 5:00pm EST

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INGREDIENTS AND APPEARANCE

ZOONO SKIN CLEAR ACNE MEDICATION 
acne medication - salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69221-301
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
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69221-301-01	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/16/2016
2	NDC: 69221-301-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/19/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	09/16/2016

Labeler - Zoono USA, LLC (073623478)

Establishment
Name	Address	ID/FEI	Business Operations
Holly Oak Chemical, Inc.		057840035	manufacture(69221-301)

Establishment
Name	Address	ID/FEI	Business Operations
Zoono USA, LLC		073623478	label(69221-301)