Label: TAURIMMUNE ESSENTIAL- tauroxicum, kali carb, phosphoricum acidum, selenium, silicea, zincum pellet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated August 26, 2019

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  • Active Ingredients

    Tauroxicum (COBAT) 4X (13.6%), 12X (1.5%), 30X (1.5%).

    Kali carbonicum 8X (13.6%), 12X (1.5%), 30X (1.5%)

    Phosphoricum acidum 8X (13.6%), 12X (1.5%), 30X (1.5%)

    Selenium metallicum 8X (13.6%), 12X (1.5%), 30X (1.5%)

    Silicea 8X (13.6%), 12X (1.5%), 30X (1.5%)

    Zincum metallicum 8X (13.6%), 12X (1.5%), 30X (1.5%)

  • Use

    For Immune support, and treatment of mild fatigue, allergies, colds, and flu.

    For Immune support, and treatment of mild fatigue, allergies, colds, and flu.

  • Directions

    Directions for adults and children 15 years of age and older: Dissolve three pellets under tongue each morning, or as directed by a health professional. Best if taken early in the day, at least 5 minutes before or after eating. See package insert for details.

  • Warnings

    Warnings

    Keep out of reach of children. Do not use if you are pregnant or breast feeding, an organ recipient, using immunosuppressive drugs, or if the tamper-evident seal is broken or missing. See package insert for details.

    Keep out of reach of children.

  • Inactive Ingredients

    Sucrose (80%), Lactose (20%).

  • Disclaimer

    Claims based on traditional
    homeopathic practice, not accepted
    medical evidence. Not FDA evaluated.

  • PRINCIPAL DISPLAY PANEL

    TaurImmune Essential

    With Taurox, An Adaptive MicroMed

    Homeopathic

    0.14 oz (4 gm)

    Essential front panel

  • INGREDIENTS AND APPEARANCE
    TAURIMMUNE ESSENTIAL 
    tauroxicum, kali carb, phosphoricum acidum, selenium, silicea, zincum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73311-109
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC8 [hp_X]
    POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE8 [hp_X]
    SELENIUM (UNII: H6241UJ22B) (SELENIUM - UNII:H6241UJ22B) SELENIUM8 [hp_X]
    ZINC CARBOBENZOXY-.BETA.-ALANYLTAURINATE (UNII: 0W4D88Q9C4) (ZINC CARBOBENZOXY-.BETA.-ALANYLTAURINATE - UNII:0W4D88Q9C4) ZINC CARBOBENZOXY-.BETA.-ALANYLTAURINATE4 [hp_X]
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE8 [hp_X]
    PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID8 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73311-109-041 in 1 BAG01/02/2015
    11 in 1 VIAL, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/02/2015
    Labeler - CureImmune Corp. (781763201)
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