Urban Wash Everday Clean Dandruff 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]

URBAN WASH EVERDAY CLEAN DANDRUFF- pyrithione zinc shampoo 
Blue Cross Laboratories, LLC

----------

Urban Wash Everday Clean Dandruff Shampoo

Active ingredient purpose

Pyrithione Zinc 0.3% Anti-dandruff

Use helps prevent recurrence of flaking and itching associated with dandruff

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

Stop use and ask doctor if

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

Warnings

For external use only

When using this product

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

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 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.

Urban Wash

Everyday Clean Dandruff Shampoo

With Pyrithione Zinc

12 FL OZ (355 mL)

Urban wash shampoo front

Urban wash shampoo back

URBAN WASH EVERDAY CLEAN DANDRUFF 
pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 22431-024
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 22431-024-01355 mL in 1 BOTTLE; Type 0: Not a Combination Product01/24/202304/07/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM03201/24/202304/07/2023
Labeler - Blue Cross Laboratories, LLC (118887378)

Revised: 6/2025