DHS BODY WASH- zinc pyrithione liquid

DHS Body Wash by

Drug Labeling and Warnings

DHS Body Wash by is a Otc medication manufactured, distributed, or labeled by Person and Covey. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Warnings

For external use only.

When using this product

• avoid contact with eyes
• If contact occurs, rinse thoroughly with water
• stop use if condition worsens or does not improve after regular use

Stop and ask a doctor if

Stop and ask a doctor if

• condition covers a large area.
• condition worsens or does not improve after regular use.

Inactive Ingredients

Water (Agua) , Triethanolamine, Laurel Sulfate, Cocamidopropyl, Hydroxysultaine, Magnesium Aluminum Silicate,
Sodium chloride, PEG-8 Distearate, Hydroxypropyl Methylcellulose, Magnesium Aluminum Silicate, Citric Acid, Sodium Hydroxide.

Keep out of the reach of children.

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

Active ingredient

Zinc Pyrithione 0.5%

Purpose

Skin protectant / Anti-seborrheic

Use

Use

• helps control and reduce the symptoms of seborrheic dermatitis.
• helps relieve flaking, scaling, redness, and itching
• helps prevent recurrence when used regularly
• Store away from excessive heat or cold.

Dosage and Administration

Directions

use daily or as directed by a doctor.
apply to wet skin.
massage into affected area.
leave on skin for several minutes
rinse thoroughly

DHS Body Wash

INGREDIENTS AND APPEARANCE

DHS BODY WASH 
zinc pyrithione liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0096-0742
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC PYRITHIONE (UNII: R953O2RHZ5) (ZINC PYRITHIONE - UNII:R953O2RHZ5)	ZINC PYRITHIONE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROXYPROPYL METHYLCELLULOSE (UNII: 3NXW29V3WO)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
TRIETHANOLAMINE LAURYL SULFATE (UNII: E8458C1KAA)
CITRIC ACID (UNII: 2968PHW8QP)
MAGNESIUM ALUMINUM SILICATE TYPE IA (UNII: SUS08ZOA9S)
WATER (UNII: 059QF0KO0R)
PEG-8 DISTEARATE (UNII: 7JNC8VN07M)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0096-0742-16	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	12/01/2025

Labeler - Person and Covey (008482473)

Establishment
Name	Address	ID/FEI	Business Operations
Person and Covey		008482473	manufacture(0096-0742)