Label: TAURIMMUNE PS- tauroxicum 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

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

View All Sections
  • Active Ingredients

    Tauroxicum (COBAT) 3X (26%), 6X (37%), 9X (37%)

  • Use

    For treatment of moderate to severe fatigue due to illness or chronic conditions. Immune support. May also help treat symptoms of colds, flu and allergies.

    For treatment of moderate to severe fatigue due to illness or chronic conditions. Immune support. May also help treat symptoms of colds, flu and allergies.

  • Directions

    Directions for adults and children 15 years of age and older: Dissolve one to three pellets under tongue once daily, 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

    PS

    Premium Strength

    TaurImmune PS

  • INGREDIENTS AND APPEARANCE
    TAURIMMUNE PS 
    tauroxicum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73311-110
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC CARBOBENZOXY-.BETA.-ALANYLTAURINATE (UNII: 0W4D88Q9C4) (ZINC CARBOBENZOXY-.BETA.-ALANYLTAURINATE - UNII:0W4D88Q9C4) ZINC CARBOBENZOXY-.BETA.-ALANYLTAURINATE6 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73311-110-111 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 (781763201)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!