Label: GLUCAMINOLYTE FORTE- glucaminolyte solution

  • NDC Code(s): 58005-402-52
  • Packager: Sparhawk Laboratories, Inc.
  • Category: OTC ANIMAL DRUG LABEL

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 May 11, 2017

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • INDICATIONS & USAGE

    SUPPLEMENTAL NUTRITIVE SOURCE

    FOR ANIMAL USE ONLY

    KEEP OUT OF REACH OF CHILDREN


    INDICATIONS

    For use as a supplemental nutritive source of electrolytes, dextrose and amino acids in cattle.

  • DOSAGE AND ADMINISTRATION

    Administer orally as a drench or by use of a stomach tube.  The usual recommended dose in adult cattle is 500 to 1000 mL, depending on size and condition.

    SHAKE WELL BEFORE USING

  • STORAGE AND HANDLING

    STORE AT CONTROLLED ROOM TEMPERATURE BETWEEN 15° and 30°C (59° - 86°)

    TAKE TIME OBSERVE LABEL DIRECTIONS

  • COMPOSITION

    Each 1000 mL of aqueous solution contains:

    Dextrose • H2O ........................... 300 g
    Sodium Chloride ........................... 5.4 g
    Sodium Acetate, Anhydrous .......... 3.0 g
    Potassium Acetate ....................... 1.0 g
    Calcium Chloride • 2H2O ........ 330.0 mg
    Magnesium Chloride • 5H2O ... 260.0 mg

    Comprised of: L-Glutamic Acid, L-Arginine, Hydrochloride, L-Proline, L-Lysine Hydrochloride, L-Leucine, L-Phnylalanine, L-Valine, L-Threonine, L-Isoleucine, L-Histidine Hydrochloride, L-Methionine, L-Tyosine, with Methylparaben (preservative) 0.18% and Propylparaben (preservative) 0.02%.

  • PRINCIPAL DISPLAY PANEL

    SLI Glucaminolyte Forte

  • INGREDIENTS AND APPEARANCE
    GLUCAMINOLYTE  FORTE
    glucaminolyte solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:58005-402
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M) (CALCIUM CATION - UNII:2M83C4R6ZB, CHLORIDE ION - UNII:Q32ZN48698) CALCIUM CHLORIDE330 mg  in 1000 mL
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE300 g  in 1000 mL
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O) (MAGNESIUM CATION - UNII:T6V3LHY838, CHLORIDE ION - UNII:Q32ZN48698) MAGNESIUM CHLORIDE260 mg  in 1000 mL
    POTASSIUM ACETATE (UNII: M911911U02) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM ACETATE1 g  in 1000 mL
    SODIUM ACETATE ANHYDROUS (UNII: NVG71ZZ7P0) (ACETATE ION - UNII:569DQM74SC, SODIUM CATION - UNII:LYR4M0NH37) SODIUM ACETATE ANHYDROUS3 g  in 1000 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698, SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE5.4 g  in 1000 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58005-402-521000 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/05/1996
    Labeler - Sparhawk Laboratories, Inc. (147979082)