A-LYTE ORAL- amino acid solution

A-Lyte by

Drug Labeling and Warnings

A-Lyte by is a Animal medication manufactured, distributed, or labeled by Durvet, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

FOR USE IN ANIMALS ONLY

KEEP OUT OF REACH OF CHILDREN

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.

DOSAGE UNDILUTED

Cattle: Administer 1 oz. A-Lyte Solution per 10 pounds of body weight in the drinking water to be consumed in one day.

Horses: Administer 10 oz. A-Lyte Solution per 100 pounds of body weight in the drinking water to be consumed in one day.

Sheep and Swine: Administer 1/2 oz. A-Lyte Solution per 5 pounds body weight in the drinking water to be consumed in one day.

STORAGE AND HANDLING

PROTECT FROM FREEZING

Store in controlled room temperature between 15o and30oC (59o-86oF).

TAKE TIME OBSERVE LABEL DIRECTIONS

COMPOSITION

Each 100 mL of aqueous solution contains:

ACTIVE INGREDIENTS:

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

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

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

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

Calcium Chloride2H2O ..................... 15 mg

INACTIVE INGREDIENTS:  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

A-LYTE  ORAL
amino acid solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 30798-001
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: 30798-001-17	500 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/11/1998

Labeler - Durvet, Inc. (056387798)