Label: CALCIUM GLUCONATE injection

  • Category: OTC 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 November 28, 2018

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  • INDICATIONS & USAGE

    INDICATIONS:  To be used as an aid in the treatment of parturient paresis (milk fever) in cattle.

  • DOSAGE & ADMINISTRATION

    DOSAGE AND ADMINISTRATION:

    Cattle:  250 mL to 500 mL.  Administer intravenously or intraperitoneally.  Solution should be warmed to body temperature and administered slowly. This product is sterile in unopened container.  It contains no preservative.  Use entire contents when first opened.  Discard any unused portion. Handle under aseptic conditions. 

    If there is no apparent improvement in the animal's condition within 24 hours, consult a veterinarian.

    EACH 100 mL CONTAINS:

    Calcium Gluconate

    (provides 2.14 grams Calcium)..........................23 grams

    Water for Injection...................................................q.s.

    Contains boric acid as a solubilizing agent.

    ELECTROLYTES PER 1000 mL:

    Calcium 1069 mEq

    Osmolarity (calc.) 6,947 m0smol/L

    Hypertonic

  • STORAGE AND HANDLING

    STORAGE: Store between 15⁰C - 30⁰C (59⁰F - 86⁰F).

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    CALCIUM GLUCONATE 
    calcium gluconate injection
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:61133-0297
    Route of AdministrationINTRAPERITONEAL, INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM GLUCONATE (UNII: SQE6VB453K) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM GLUCONATE23 g  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61133-0297-7500 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/23/2005
    Labeler - Bimeda, Inc. (060492923)
    Registrant - Bimeda, Inc. (060492923)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bimeda-MTC256232216manufacture