ZO SKIN HEALTH ASTRINGENT SOLUTION- aluminum acetate powder

ZO Skin Health Astringent Solution by

Drug Labeling and Warnings

ZO Skin Health Astringent Solution by is a Otc medication manufactured, distributed, or labeled by ZO Skin Health, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

• Active Ingredients: Purpose
• Aluminum Sulfate Tetradecahydrate, 2850 mg: Astringent*
• Calcium AcetateMonohydrate, 2016 mg: Astringent*

*When combined together in water, these ingredients form the active ingredient aluminum acetate. See Directions

Uses

For temporary relief of minor skin irritations due to rashes caused by soaps, detergents, cosmetics, or jewelry.

Warnings

For external use only.

When using this product

■ avoid contact with eyes. If contact occurs, rinse thoroughly with water.

■ do not cover compress or wet dressing with plastic to prevent evaporation

■ in some skin conditions, soaking too long may overdry

Stop use and ask a doctor

■ if condition worsens or symptoms persist for more than 7 days

Keep out of reach of children.

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

Directions

For powder dosage form:

■ dissolve 1 packet in 12 oz. of cool or warm water
■ stir until fully dissolved; do not strain or filter. The resulting mixture contains 0.45% aluminum acetate and is ready for use.
For use as a compress or wet dressing:
■ soak a clean, soft cloth in the solution
■ apply cloth loosely to affected area for
15 to 30 minutes
■ repeat as needed or as directed by a doctor
■ discard solution after each use

Other Information

■ Protect this product from excessive heat and direct sun

Inactive Ingredients

Avena Sativa (Oat) Kernel Protein, Chitosan, Dextrin, Hydrolyzed Soy Protein, Potassium Sorbate, Whey Protein.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZO SKIN HEALTH ASTRINGENT SOLUTION 
aluminum acetate powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42851-090
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM ACETATE (UNII: 80EHD8I43D) (ALUMINUM CATION - UNII:3XHB1D032B)	ALUMINUM ACETATE	4866 mg  in 6 g

Inactive Ingredients
Ingredient Name	Strength
WHEY (UNII: 8617Z5FMF6)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42851-090-06	6 g in 1 PACKET; Type 0: Not a Combination Product	02/21/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	02/21/2022

Labeler - ZO Skin Health, Inc. (826468527)