DOUBLE A ORAL- amino acid solution

Double A by

Drug Labeling and Warnings

Double A by is a Animal medication manufactured, distributed, or labeled by Vedco, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

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.

INDICATIONS

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

DOSAGE

For use in drinking water.  Supply fresh water daily.

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

Horses: Administer 10 oz. Double "A" Solution per 100 pounds body weight in the drinking water consumed in one day.

Sheep and Swine: Administer 1/2 oz. per 5 pounds body weight i the drinking water consume in one day.

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:

DextroseH2O ....................................... 5 g

Sodium Acetate3H2O ..................... 250 mg

Magnesium Sulfate7H2O .................. 20 mg

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

Calcium Chloride2H2O ..................... 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

DOUBLE A  ORAL
amino acid solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 50989-101
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: 50989-101-25	500 mL in 1 BOTTLE
2	NDC: 50989-101-17	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 - Vedco, Inc. (021634266)