AMINO ACID- amino acid 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.

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AMINO ACID ORAL CONCENTRATE

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 30oC (59o-86oF).

PX-AA Oral Conc-20

AMINO ACID 
amino acid concentrate
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:57319-526
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:57319-526-04500 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/01/2007
Labeler - PHOENIX (150711039)

Revised: 2/2020
Document Id: 9aaacb67-990f-42d7-8adb-3bfc422b8110
Set id: c9efc096-145f-47d6-b01a-849e755bd2e2
Version: 1
Effective Time: 20200212
 
PHOENIX