RENAKARE- potassium gluconate powder

RenaKare by

Drug Labeling and Warnings

RenaKare by is a Animal medication manufactured, distributed, or labeled by Neogen Corporation-Mercer Rd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DESCRIPTION

RenaKare™

Potassium Gluconate Powder

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

​FOR ANIMAL USE ONLY

​Each level ¼ teaspoon (0.65 g) contains (minimum):

Potassium gluconate......................2 mEq (468 mg)

in a palatable base

​Dosage:

Adult cats and dogs..............2 mEq/4.5 kg (¼ tsp/10 lb) PO BID

Kittens and puppies..............Consult veterinarian

Administer with food. Dosage may be adjusted as necessary by the veterinarian.

​Store in a dry place at controlled room temperature 15°-30°C (59°-86°F). Keep container tightly closed.

SPL UNCLASSIFIED SECTION

Item No. 09075

​KEEP OUT OF REACH OF CHILDREN

​Indications:

For use as a potassium supplement in hypokalemic cats and dogs.

​Warnings:

May cause hyperkalemia. Do not exceed the recommended dose. Frequent patient monitoring is advised. Adverse effects include gastrointestinal irritation, muscular weakness, twitching, irritability, and cardiac conduction distrubances. Potassium salts are contraindicated in animals with hyperkalemia, severe renal impairment or failure, sever hemolytic reactions, Addison's disease, decreased gastrointestinal motility, and acute dehydration.

​Precaustions:

Use with caution in animals receiving digoxin, potassium-sparing diuretics, ACE inhibitors, and NSAIDS.

SPL UNCLASSIFIED SECTION

Lot No.:

Exp. Date:

Manufactured by Neogen Corporation

Lexington, KY 40511 USA 859/254-1221

L592-91908

PRINCIPAL DISPLAY PANEL - 4 oz Bottle

NDC: 59051-9075-1

RenaKare™

Potassium Gluconate Powder

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

NEOGEN.Vet

Net Contents: 4 oz

INGREDIENTS AND APPEARANCE

RENAKARE 
potassium gluconate powder

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 59051-9075
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM GLUCONATE (UNII: 12H3K5QKN9) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM GLUCONATE	468 mg  in 0.65 g

Product Characteristics
Color	brown	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59051-9075-1	113 g in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/24/2012

Labeler - Neogen Corporation-Mercer Rd (042125879)

Establishment
Name	Address	ID/FEI	Business Operations
Neogen Corporation-Mercer Rd		042125879	analysis, manufacture, label