Label: AMINO ACID concentrate

  • NDC Code(s): 57561-102-06
  • Packager: Agri Laboratoies, Ltd.
  • 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 June 19, 2017

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  • INDICATIONS & USAGE

    ORAL SOLUTION

    For Animal Use Only

    Keep Out of Reach of Children

    INDICATIONS

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

  • DOSAGE UNDILUTED

    Administer orally as a drench. The usual recommended dose in adult cattle and horses is 50 to 500 mL, depending on size and condition.

    Not for Human use

  • STORAGE AND HANDLING

    STORE BETWEEN 15o and 30o C (59o and 86oF)

    TAKE TIME OBSERVE LABEL DIRECTIONS

  • CONTENTS

    Each 100 mL of aqueous solution contains:

    Dextrose • H2O .......................... 5 g
    Sodium Acetate • 3H2O ........ 250 mg
    Magnesium Sulfate • 7H2O ... 200 mg
    Potassium Chloride .............. 200 mg
    Calcium Chloride • 2H2O .......150 mg

    Comprised of : Niacinamide, Pyridoxine Hydrochloride (B6), Thiamine Hydrochloride (B1), d-Panthenol, Riboflavin (B2), Cyanocobalamin (B12), L-Leucine, L-Lysine Hydrochloride, L-Glutamic Acid, L-Valine, L-Phenylalanine, L-Arginine Hydrochloride, L-Isoleucine, L-Threonine, L-Histidine Hydrochloride • H2O, L-Methionine, L-Cysteine Hydrochloride • H2O, with propylne glycol 2.5%, sorbitol 2.5%, lactic acid 0.16%, citric acid 0.1%, BHA 0.005%, methylparaben 0.18%, propylparaben 0.02%, and ehtylparaben 0.01% (preservatives).

  • PRINCIPAL DISPLAY PANEL

    AL AA Oral Concentrate

  • INGREDIENTS AND APPEARANCE
    AMINO ACID 
    amino acid concentrate
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:57561-102
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CHLORIDE ANHYDROUS (UNII: OFM21057LP) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION150 mg  in 100 mL
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE5 g  in 100 mL
    MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM SULFATE HEPTAHYDRATE200 mg  in 100 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (CHLORIDE ION - UNII:Q32ZN48698, POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE200 mg  in 100 mL
    SODIUM ACETATE ANHYDROUS (UNII: NVG71ZZ7P0) (SODIUM CATION - UNII:LYR4M0NH37, ACETATE ION - UNII:569DQM74SC) SODIUM ACETATE ANHYDROUS250 mg  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57561-102-06500 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/01/1991
    Labeler - Agri Laboratoies, Ltd. (155594450)