Label: AMINO ACID ORAL- amino acid solution

  • NDC Code(s): 11695-4120-7
  • Packager: Covetrus North America
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated January 6, 2021

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  • INDICATIONS & USAGE

    A combination of amino acids, B-vitamins, electrolytes and dextrose

    For animl use only

    Keep out of reach of children

    Indications

    For use as a supplemental nutritive source of amino acids, electrolytes, B complex vitamins, and dextrose for cattle and horses.

  • Dosage and administration

    Administer orally as a drench or by use of a stomach tube.  The usual recommended dose in adult cattle and horses is 500 to 3000 mL, depending on size and condition.

  • STORAGE AND HANDLING

    Store at 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, thiamine HCl, d-Panthenol, Riboflavin, 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

    COV-AA Plus Oral Solution

  • INGREDIENTS AND APPEARANCE
    AMINO ACID   ORAL
    amino acid solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:11695-4120
    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:11695-4120-71000 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/01/1996
    Labeler - Covetrus North America (603750329)