DANDRUFF SHAMPOO (PYRITHIONE ZINC) LOTION/SHAMPOO [CARDINAL HEALTH]

DANDRUFF SHAMPOO (PYRITHIONE ZINC) LOTION/SHAMPOO [CARDINAL HEALTH]
PDF | XML

NDC 37205-311-15
Set ID 61b3e7ce-3c2a-4bb8-bd21-9b92e30b0819
Category HUMAN OTC DRUG LABEL
Packager Cardinal Health
Generic Name
Product Class
Product Number
Application Number PART358
  • ACTIVE INGREDIENT

    Active ingredient                      Purpose

    Pyrithione Zinc   1%                          Anti-Dandruff

  • INDICATIONS & USAGE

    Use  helps prevent recurrence of flaking and itching associated with dandruff

  • WARNINGS

    Warnings
    For external use only

    When using this product
    •do not get into eyes.  If contact occurs, rinse eyes thoroughly with water.

    Stop use and ask a doctor if
    • condition worsens or does not improve after regular use as directed

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

    Directions
    • shake well • for maximum dandruff control, use every time you shampoo • wet hair, message onto scalp, rinse, repeat if desired
    • for best result use at least twice a week or as directed by doctor
  • INACTIVE INGREDIENT

    Inactive ingredients water, sodium laureth sulfate, glycol distearate, sodium lauryl sulfate, cocamidopropyl betaine, cocamide MEA,
    zinc carbonate, behentrimonium chloride, fragrance, magnesium sulfate, sodium benzoate, zinc chloride, sodium citrate, benzyl alcohol, sodium chloride, sodium hydroxide, blue 1, red 4
  • PRINCIPAL DISPLAY PANEL

    Compare to
    Head + Shoulders
    active ingredient
    Pyrithione Zinc
    Dandruff
    Shampoo
    Everyday Clean
    Everyday basi cleaning
    for Normal or Oily Hair
    14.2 FL OZ
    (420 mL)
    image of package label

  • INGREDIENTS AND APPEARANCE
    DANDRUFF SHAMPOO 
    pyrithione zinc lotion/shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37205-311
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC1 kg  in 100 L
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    ZINC CARBONATE (UNII: EQR32Y7H0M)  
    BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    ZINC (UNII: J41CSQ7QDS)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37205-311-15.42 L in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35805/19/1998
    Labeler - Cardinal Health (097537435)
    Registrant - Vi Jon (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi Jon790752542manufacture

Related Drugs