Label: EQUALINE MOISTURIZING DANDRUFF MEDICATED FORMULA- selenium sulfide shampoo

  • 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 October 15, 2010

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  • Active Ingredient

    Selenium Sulfide 1%

  • Purpose

    Anti-Dandruff

  • Uses

    For relief of flaking, and itching associated with dandruff and seborrheic dermatitis and to help prevent the chance of re-occurence

  • Warnings

    For external use only

    Ask a doctor before using if you have

    Seborrheic dermatitis in areas other than the scalp

    When using this product

    avoid contact with eyes. If contact occurs, rinse with water. For use on color treated or permed hair, rinse thoroughly

    Stop using this product and ask doctor if

    condition worsens or does not improve after regular use of this product as directed

    Keep out of reach of children

    In case of accidental ingestion, get medical help or contact a Poison Control Center immediately

  • Directions

    • Shake well, apply shampoo, rinse thoroughly
    • For best results, use at least twice a week or as directed by a doctor
  • Questions? Comments?

    1 - 877 - 932 - 7948

  • Inactive Ingredients

    Water (Aqua), Ammonium Lauryl Sulfate, Ammonium Laureth Sulfate, Dihydrogenated Tallow Phthalic Acid Amide, Cocamide DEA, Fragrance (Parfum), Titanium Dioxide, Dimethicone, Hydroxypropyl Methylcellulose, Citric Acid, Sodium Isostearoyl Lactylate, DMDM Hydantoin, Aloe Barbadensis Leaf Juice, Sodium Citrate, Sodium Chloride, Blue 1 (CI 42090)

  • Package Front and Back Labels

    ra11.jpg
    11OZ front and back labels
  • INGREDIENTS AND APPEARANCE
    EQUALINE MOISTURIZING DANDRUFF  MEDICATED FORMULA
    selenium sulfide shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-611
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM - UNII:H6241UJ22B) SELENIUM SULFIDE1 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6)  
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    HYPROMELLOSE 2208 (100 MPA.S) (UNII: B1QE5P712K)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM ISOSTEAROYL LACTYLATE (UNII: 8730J0D3EV)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41163-611-11325 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart358H10/15/2010
    Labeler - Supervalu Inc (006961411)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture
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