Label: CALCIUM GLUCONATE- calcium gluconate injection 

  • Label RSS
  • NDC Code(s): 61133-0297-7
  • Packager: Bimeda, Inc., Division of Cross Vetpharm Group
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 07/13

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  • INDICATIONS & USAGE

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

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  • 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

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  • STORAGE AND HANDLING

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

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  • INGREDIENTS AND APPEARANCE
    CALCIUM GLUCONATE 
    calcium gluconate injection
    Product Information
    Product Type OTC ANIMAL DRUG LABEL Item Code (Source) NDC:61133-0297
    Route of Administration INTRAPERITONEAL, INTRAVENOUS DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CALCIUM GLUCONATE (CALCIUM CATION) CALCIUM GLUCONATE 23 g  in 100 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:61133-0297-7 500 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 03/23/2005
    Labeler - Bimeda, Inc., Division of Cross Vetpharm Group (060492923)
    Registrant - Bimeda, Inc. Division of Cross Vetpharm Group (060492923)
    Establishment
    Name Address ID/FEI Business Operations
    Bimeda-MTC., Division of Cross Vetpharm Group 256232216 manufacture
    Establishment
    Name Address ID/FEI Business Operations
    Zhejiang Ruibang 544807456 api manufacture
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