AMINO ACID: Product Information

AMINO ACID- calcium chloride anhydrous, dextrose monohydrate, magnesium sulfate heptahydrate, potassium chloride and sodium acetate anhydrous concentrate
PHOENIX

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.

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.

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

PX-AA Oral Conc-20
(click image for full-size original)

AMINO ACID
amino acid concentrate
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:57319-526
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CALCIUM CHLORIDE ANHYDROUS (CALCIUM CATION) CALCIUM CATION 150 mg in 100 mL
DEXTROSE MONOHYDRATE (ANHYDROUS DEXTROSE) DEXTROSE MONOHYDRATE 5 g in 100 mL
MAGNESIUM SULFATE HEPTAHYDRATE (MAGNESIUM CATION) MAGNESIUM SULFATE HEPTAHYDRATE 200 mg in 100 mL
POTASSIUM CHLORIDE (CHLORIDE ION and POTASSIUM CATION) POTASSIUM CHLORIDE 200 mg in 100 mL
SODIUM ACETATE ANHYDROUS (SODIUM CATION and ACETATE ION) SODIUM ACETATE ANHYDROUS 250 mg in 100 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:57319-526-04 500 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 03/01/2007
Labeler — PHOENIX (150711039)

Revised: 02/2020 PHOENIX

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