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Medicated Dandruff (Dolgencorp.LLC)

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SHAMPOO .325 L in 1 BOTTLE, PLASTIC (55910-246-39) Label Information

Complete Medicated Dandruff Information

  • ACTIVE INGREDIENT

    Active ingredient
    Selenium sulfide 1%

    Purpose
    Anti-Dandruff

  • INDICATIONS & USAGE

    Use for relief of itching and flaking associated with dandruff and seborrheic dermatitis and to help prevent reoccurrence

  • WARNINGS

    Warnings
    For external use only

    Ask a doctor before use if you have seborrheic dermatitis in areas other than the scalp

    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, bet medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions Shake well wet hair, massage onto scalp, rinse thoroughly
    for best results use at least twice a week or as directed b a doctor

  • OTHER SAFETY INFORMATION

    Other information for color-treated or permed hair, rinse extra thoroughly

  • INACTIVE INGREDIENT

    Inactive ingredients water, ammonium laury sulfate, TEA-lauryl sulfate, ammonium laureth sulfate,  cocamidopropyl betaine, magnesium aluminum silicate, fragrance,
    menthol, cocamide DEA, DMDM hydantoin citric acid, hydroxypropyl methylcellulose, xanthan gum, cellulose gum, FD+C blue no. 1, D+C red no 33, sodium citrate, sodium chloride.

  • ADVERSE REACTIONS

    PACKAGED FOR DOLGENCORP, LLC
    100 MISSION RIDGE, GOODLETTSVILLE, TN 37072 USA
    visit us at Rexall.com or call 1-866-4-REXALL

  • PRINCIPAL DISPLAY PANEL

    Since 1903
    Rexall
    MAXIMUM
    DANDRUFF
    CONTROL
    SHAMPOO
    Selenium Sulfide
    Dandruff Shampoo
    For a healthier scalp and hair
    Helps prevent flakes
    11 FL OZ (325 mL)
    image of principal display package

  • INGREDIENTS AND APPEARANCE
    MEDICATED DANDRUFF 
    selenium sulfide shampoo
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-246
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM SULFIDE - UNII:Z69D9E381Q) SELENIUM SULFIDE 1 kg  in 100 L
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    TROLAMINE LAURYL SULFATE (UNII: E8458C1KAA)  
    AMMONIUM LAURETH-3 SULFATE (UNII: 896SJ235FN)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    MENTHOL (UNII: L7T10EIP3A)  
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:55910-246-39 .325 L in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part358H 11/03/2011
    Labeler - Dolgencorp.LLC (068331990)
    Registrant - Vi-Jon (088520668)
    Establishment
    Name Address ID/FEI Business Operations
    Vi-Jon 088520668 manufacture