AMINO ACID by PHOENIX AMINO ACID concentrate

AMINO ACID by

Drug Labeling and Warnings

AMINO ACID by is a Animal medication manufactured, distributed, or labeled by PHOENIX. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

COMPONENTS

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

INDICATIONS

COMPOSITIION

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).

INDICATIONS

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

DOSAGE UNDILUTED

CATTLE:  Administer 1 oz. Amino Acid Concentrate per 100 pounds body weight in drinking water to be consumed in one day.

HORSE:  Administer 10 oz. Amino Acid Concentrate per 1000 pounds body weight in drinking water to be consumed in one day. 

SHEEP and SWINE:  Administer 1/2 oz. Amino Acid Concentrate per 50 pounds body weight in drinking water to be consumed in one day.

STORAGE AND HANDLING

STORE AT COMTROLLED ROOM TEMPERATAURE BETWEEN 15o AND 30oC (59o-86oF).

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AMINO ACID 
amino acid concentrate

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 57319-526
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CHLORIDE ANHYDROUS (UNII: OFM21057LP) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CATION	150 mg  in 100 mL
DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK)	DEXTROSE MONOHYDRATE	5 g  in 100 mL
MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM SULFATE HEPTAHYDRATE	200 mg  in 100 mL
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (CHLORIDE ION - UNII:Q32ZN48698, POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CHLORIDE	200 mg  in 100 mL
SODIUM ACETATE ANHYDROUS (UNII: NVG71ZZ7P0) (SODIUM CATION - UNII:LYR4M0NH37, ACETATE ION - UNII:569DQM74SC)	SODIUM ACETATE ANHYDROUS	250 mg  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57319-526-04	500 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/01/2007

Labeler - PHOENIX (150711039)