Label: A-LYTE ORAL- amino acid solution

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

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Drug Label Information

Updated January 4, 2017

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  • INDICATIONS & USAGE

    FOR USE IN ANIMALS ONLY

    KEEP OUT OF REACH OF CHILDREN

    An oral source of vitamins, amino acids and electrolytes for cattle, swine, sheep and horses when dietary intake is reduced.

    For use in drinking water

    Supply fresh drinking water daily.

  • DOSAGE UNDILUTED

    Cattle: Administer 1 oz. A-Lyte Solution per 10 pounds of body weight in the drinking water to be consumed in one day.

    Horses: Administer 10 oz. A-Lyte Solution per 100 pounds of body weight in the drinking water to be consumed in one day.

    Sheep and Swine: Administer 1/2 oz. A-Lyte Solution per 5 pounds body weight in the drinking water to be consumed in one day.

  • STORAGE AND HANDLING

    PROTECT FROM FREEZING

    Store in controlled room temperature between 15o and30oC (59o-86oF).

    TAKE TIME OBSERVE LABEL DIRECTIONS

  • COMPOSITION

    Each 100 mL of aqueous solution contains:

    ACTIVE INGREDIENTS:

    Dextrose•H2O ....................................... 5 g

    Sodium Acetate•3H2O ..................... 250 mg

    Magnesium Sulfate•7H2O .................. 20 mg

    Potassium Chloride ........................... 20 mg

    Calcium Chloride•2H2O ..................... 15 mg

    INACTIVE INGREDIENTS:  Niacinamide,  Pyridoxine HCl (B6), d-Panthenol,  Riboflavin (B2), Cyanocobalamin (B12), L-Argenine HCl, L-Cysteine HCl H2O, L-Glutamic Acid, L-Histidine HCl H2O, L-Isoleucie, L-Leucine, L-Lycine HCl, L-Methionine, L-Phenylalamine, L-Theonine, L-Valine with Methylparaben 0.18%, Ethylparaben 0.01%, Propylparaben 0.02%.

  • PRINCIPAL DISPLAY PANEL

    AA Solution

  • INGREDIENTS AND APPEARANCE
    A-LYTE  ORAL
    amino acid solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:30798-001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE5000 mg  in 100 mL
    CALCIUM CHLORIDE ANHYDROUS (UNII: OFM21057LP) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION15 mg  in 100 mL
    MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM SULFATE HEPTAHYDRATE20  mg  in 100 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698) POTASSIUM CHLORIDE20 mg  in 100 mL
    SODIUM ACETATE ANHYDROUS (UNII: NVG71ZZ7P0) (ACETATE ION - UNII:569DQM74SC, SODIUM CATION - UNII:LYR4M0NH37) SODIUM ACETATE ANHYDROUS250 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    VALINE (UNII: HG18B9YRS7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30798-001-17500 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/11/1998
    Labeler - Durvet, Inc. (056387798)