Label: AMINO ACID ORAL- amino acid solution
- NDC Code(s): 58005-101-25, 58005-101-52
- 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 January 5, 2017
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- INDICATIONS & USAGE
-
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
-
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
-
INGREDIENTS AND APPEARANCE
AMINO ACID ORAL
amino acid solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:58005-101 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 5000 mg in 100 mL CALCIUM CHLORIDE ANHYDROUS (UNII: OFM21057LP) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 15 mg in 100 mL MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM SULFATE HEPTAHYDRATE 20 mg in 100 mL POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698) POTASSIUM CHLORIDE 20 mg in 100 mL SODIUM ACETATE ANHYDROUS (UNII: NVG71ZZ7P0) (ACETATE ION - UNII:569DQM74SC, SODIUM CATION - UNII:LYR4M0NH37) SODIUM ACETATE ANHYDROUS 250 mg in 100 mL Inactive Ingredients Ingredient Name Strength VALINE (UNII: HG18B9YRS7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58005-101-25 500 mL in 1 BOTTLE 2 NDC:58005-101-52 1000 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/01/1998 Labeler - Sparhawk Laboratories, Inc. (147979082)