Label: AMINO ACID concentrate
- NDC Code(s): 57319-526-04
- Packager: PHOENIX
- Category: OTC ANIMAL DRUG LABEL
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Drug Label Information
Updated February 12, 2020
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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 mgComprised 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
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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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AMINO ACID
amino acid concentrateProduct 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)
