Label: AMINO ACID ORAL- amino acid solution

  • 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 January 17, 2018

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  • INDICATIONS & USAGE

    Supplemental Nutritive Source

    For animal use only.

    Keep out of reach of children.


    INDICATIONS

    For use as a nutritional supplement of vitamins, amino acids and electrolytes for cattle, swine, sheep and horses.

  • DOSAGE AND ADMINISTRATION

    For use in drinking water.  Supply fresh water daily.

    Cattle: Administer 1 oz. per 10 pounds body weight in the drinking water consumed in one day.

    Horses: Administer 10 ozs. per 100 pounds body weight in the drinking water consumed in one day.

    Sheep and Swine: Administer 1 oz. per 10 pounds body weight i the drinking water consume in one day.

  • STORAGE AND HANDLING

    PROTECT FROM LIGHT.

    Store in controlled room temperature between 15o and 30oC (59o-86oF).

    TAKE TIME OBSERVE LABEL DIRECTIONS

  • COMPOSITION

    Each 100 mL of aqueous solution contains:

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

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

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

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

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

    Comprised of: 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

    V1 AAOral Sol Unit

  • INGREDIENTS AND APPEARANCE
    AMINO ACID   ORAL
    amino acid solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:13985-101
    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:13985-101-25500 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/17/2011
    Labeler - MWI/VetOne (019926120)