Label: IMMUZIM- echinacea angustifolia root and echinacea pallida root extract

  • Category: PRESCRIPTION ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated April 19, 2010

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

View All Sections
  • SPL UNCLASSIFIED SECTION

    Echinacea Sp.

  • Active Ingredients:

    Echinacea [Echinacea angustifolia] 7.5mg per ml
    Echinacea [Echinacea pallida] 7.5mg per ml

  • Inactive Ingredients:

    Acetic acid glacial and Propionic acid [organic preservatives[Salt,Water

  • WARNINGS

    FOR USE ON ANIMALS ONLY

  • SPL UNCLASSIFIED SECTION

    Immuzim contains NO animal parts or residues

    Imported to the USA by :
    Emerald Valley Natural Health Inc, Exeter, NH 03833

    Batch No: 94414
    Use by Date: 03/12/11

    Immuzim is manufactured in the UK by
    SCA Nutec [Provimi Ltd]
    Nutec Mill, Eastern Avenue
    Lichfield, Staffordshire, WS13 7SE, UK

    Exported by :
    Equiglobal Ltd
    Manningtree, Essex, CO11 1UT, UK

    20 Litres/5.283 gallons [US]

  • PRINCIPAL DISPLAY PANEL

    image of container

  • INGREDIENTS AND APPEARANCE
    IMMUZIM 
    echinacea angustifolia root and echinacea pallida root extract
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:52338-398
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ECHINACEA ANGUSTIFOLIA ROOT (UNII: D982V7VT3P) (ECHINACEA ANGUSTIFOLIA ROOT - UNII:D982V7VT3P) ECHINACEA ANGUSTIFOLIA ROOT7.5   in 1 mL
    ECHINACEA PALLIDA ROOT (UNII: MGY2W95GWO) (ECHINACEA PALLIDA ROOT - UNII:MGY2W95GWO) ECHINACEA PALLIDA ROOT7.5   in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52338-398-2020000 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/01/2010
    Labeler - SCA NuTec (233072193)
    Establishment
    NameAddressID/FEIBusiness Operations
    SCA NuTec233072193manufacture
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events (Animal Drug), FDA Safety Recalls (Animal Drug)

Related Resources

Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

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