Label: URBAN WASH EVERDAY CLEAN DANDRUFF- pyrithione zinc shampoo

  • NDC Code(s): 22431-024-01
  • Packager: Blue Cross Laboratories, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 17, 2023

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  • 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)

    Urban wash shampoo front

    Urban wash shampoo back

  • INGREDIENTS AND APPEARANCE
    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 Product01/24/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM03201/24/2023
    Labeler - Blue Cross Laboratories, LLC (118887378)
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