Label: ETERNAL SPIRIT BEAUTY HAIR PRO ANTI-DANDRUFF- zinc pyrithione shampoo

  • NDC Code(s): 70947-001-10
  • Packager: Worldwide Cosmetics, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 12, 2024

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Zinc Pyrithione 1%

  • PURPOSE

    Anti-Dandruff

  • Use

    Helps prevent recurrence of flaking and itching associated with dandruff

  • WARNINGS

    For external use only.

    Do not use on wounds or damaged skin or on a child under 12 years of age unless directed by a physician.

  • WHEN USING

    Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water

  • STOP USE

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

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical help, or contact Poison Control Center right away

  • Directions

    For maximum dandruff control, use every time you shampoo
    Wet hair, massage onto scalp, rinse, and repeat if desired

    For best results, use at least twice a week or as directed by a doctor

  • OTHER INFORMATION

    See on the bottom of the bottle for lot number and expiration date.

  • INACTIVE INGREDIENT

    Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Cocamidopropylamine Oxide, Cocamide MEA, Propylene Glycol, Fragrance (Parfum), Aloe Vera (Aloe Barbadensis) Leaf Juice, Acrylates/Steareth-20 Methacrylate Copolymer, DMDM Hydantoin, Malus Domestica Fruit Cell Culture Extract, Xanthan Gum, Sodium Benzoate, Propylparaben, Methylparaben, Phosphoric Acid, Polyquaternium-7, FD&C Blue No.1 (CI 42090), Linalool, Butylphenyl Methylpropional, Limonene

  • Questions or comments?

    Contact us +1-305-468-8270

  • ETERNAL SPIRIT BEAUTY - HAIR PRO ANTIDANDRUFF SHAMPOO AND CONDITIONER

    ETERNAL 2 IN 1

  • INGREDIENTS AND APPEARANCE
    ETERNAL SPIRIT BEAUTY HAIR PRO ANTI-DANDRUFF 
    zinc pyrithione shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70947-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    APPLE (UNII: B423VGH5S9)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)  
    LIMONENE, (+/-)- (UNII: 9MC3I34447)  
    WATER (UNII: 059QF0KO0R)  
    POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 900 KD) (UNII: B70CUU14M9)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    ETHYL ACRYLATE/METHACRYLIC ACID/STEARETH-20 METHACRYLATE COPOLYMER (UNII: EPA1872R1N)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    PHOSPHORIC ACID (UNII: E4GA8884NN)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70947-001-10295.7 mL in 1 BOTTLE; Type 0: Not a Combination Product09/08/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03204/07/2021
    Labeler - Worldwide Cosmetics, Inc (013176366)