Label: CVS GOLD- selenium sulfide shampoo

  • NDC Code(s): 63148-209-13
  • Packager: Apollo Health and Beauty Care
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 2024

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  • Active Ingredient

    Selenium Sulfide 1%

  • Purpose

    Anti-dandruff Anti-seborrheic dermatitis

  • Uses

    Helps prevent recurrence of flaking and itching associated with dandruff and seborrheic dermatitis.

  • Warnings

    For external use only

    Ask a doctor before use if you have a condition that covers a large area of the body.

    When using this product avoid contact with 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 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

    • Apply a generous amount to wet hair, massage onto scalp and work evenly to the ends.
    • Leave on for 3-5 minutes.
    • Rinse thoroughly.
    • For best results use at least twice a week or as directed by a doctor.
  • Inactive Ingredients

    Acrylate Copolymer, Caprylyl Glycol, Citric Acid, Cocamidopropyl Betaine, Dimethicone, Fragrance (Parfum), Glycol Stearate, Honey, Hydroxypropyl Methylcellulose, Phenoxyethanol, Red 4 (CI 14700), Sodium Chloride, Sodium Citrate, Sodium Hydroxide, Sodium Laureth Sulfate, Tetrasodium EDTA, Water (Aqua).

  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    CVS GOLD 
    selenium sulfide shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63148-209
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM SULFIDE - UNII:Z69D9E381Q) SELENIUM SULFIDE1000 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CITRIC ACID (UNII: 2968PHW8QP)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    RED 4 (UNII: X3W0AM1JLX)  
    TETRASODIUM EDTA (UNII: MP1J8420LU)  
    ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    HONEY (UNII: Y9H1V576FH)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    HYDROXYPROPYL METHYLCELLULOSE (UNII: 3NXW29V3WO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63148-209-13400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/02/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03212/02/2024
    Labeler - Apollo Health and Beauty Care (201901209)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture(63148-209)
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