RENAKARE GEL- potassium gluconate gel

RenaKare by

Drug Labeling and Warnings

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

Drug Details [pdf]

DESCRIPTION

RenaKare™

Gel

Potassium Gluconate

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

WARNINGS

FOR ANIMAL USE ONLY

DESCRIPTION

Each 1/2 teaspoon (2.34 g) contains (minimum):
Potassium gluconate............2 mEq (468 mg)
In a palatable base

DOSAGE & ADMINISTRATION

Dosage:
Adult cats and dogs.....2 mEq/4.5 kg
(½ tsp/10 lb) PO BID

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

Administer with food. Gel is highly palatable. Place small amount on animal’s nose or in mouth to initiate interest. Place gel on food or on animal’s paw thereafter. Dosage may be adjusted as necessary by the veterinarian.

STORAGE AND HANDLING

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

SPL UNCLASSIFIED SECTION

UPC
726087 09076 4

​KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

Indications:

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

WARNINGS AND PRECAUTIONS

Warnings:

Do no administer in diseases where high potassium levels may be encountered, such as severe renal insufficiency or adrenal insufficiency.

Precaution:

Use with caution in the presence of cardiac disease, particularly in digitalized patients or in the presence of renal disease.

SPL UNCLASSIFIED SECTION

Manufactured for Neogen Corporation

Lexington, KY 40511 USA 859/254-1221

PRINCIPAL DISPLAY PANEL - 5 oz Bottle

NDC: 59051-9076-6

RenaKare™

Gel

Potassium Gluconate

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

NEOGEN® Vet

Net Contents: 5 oz (142 g)

INGREDIENTS AND APPEARANCE

RENAKARE  GEL
potassium gluconate gel

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 59051-9076
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 234 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: 59051-9076-6	142 g in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/01/2000

Labeler - Neogen Corporation-Mercer Rd (042125879)

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

Establishment
Name	Address	ID/FEI	Business Operations
Jungbunzlauer Ladenburg GmbH		322121609	api manufacture