URBAN WASH EVERDAY CLEAN DANDRUFF- pyrithione zinc shampoo

Urban Wash Everday Clean Dandruff by

Drug Labeling and Warnings

Urban Wash Everday Clean Dandruff by is a Otc medication manufactured, distributed, or labeled by Blue Cross Laboratories, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient purpose

Pyrithione Zinc 0.3% Anti-dandruff

PURPOSE

Use helps prevent recurrence of flaking and itching associated with dandruff

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Stop use and ask doctor if

• conditions worsens or does not improve after regular use as directed

WARNINGS

Warnings

For external use only

When using this product

• do not get into eyes. If contact occurs, rinse eyes thoroughly with water

DOSAGE & ADMINISTRATION

Directions

• shake well
• for maximum dandruff control, use everytime you shampoo
• wet hair massage onto scalp rinse repeat if desired
• for best results use at least twice a week or as directed by a doctor

INACTIVE INGREDIENT

Inactive ingredients Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Cocamide DIPA, Glycerin, Styrene Acrylic Copolymer, Sodium Chloride, Alkyl Poly Glucocide, Glycol Distearate, Cocamide MIPA, Benzyl Alcohol, Tetrasodium EDTA, Sodium Hydroxide, Fragrance, Methylchloroisothiazolinone, Methylisothiazolinone.

PRINCIPAL DISPLAY PANEL

Urban Wash

Everyday Clean Dandruff Shampoo

With Pyrithione Zinc

12 FL OZ (355 mL)

INGREDIENTS AND APPEARANCE

URBAN WASH EVERDAY CLEAN DANDRUFF 
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22431-024
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	0.3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM HYDROXIDE (UNII: 55X04QC32I)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
WATER (UNII: 059QF0KO0R)
BENZYL ALCOHOL (UNII: LKG8494WBH)
EDETATE SODIUM (UNII: MP1J8420LU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22431-024-01	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/24/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	M032	01/24/2023

Labeler - Blue Cross Laboratories, LLC (118887378)