RENAPLUS- potassium gluconate powder

RenaPlus by

Drug Labeling and Warnings

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

Drug Details [pdf]

RenaPlus™ Powder

​Potassium Gluconate

Keep out of reach of children.

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

USE IN SPECIFIC POPULATIONS

​FOR USE IN ANIMALS ONLY

​Each 0.65 g (1/4 level teaspoon) contains a minimum:

Potassium gluconate..............................2 mEq (468 mg) in a palatable base.

Dosage:

The suggested dose of RenaPlus for adult cats and dogs is 0.65 g (1/4 level teaspoon) per 10 lb (4.5 kg) body weight twice daily with food. Dosage may be adjusted to satisfy patient's need.

​Precautions:

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

SPL UNCLASSIFIED SECTION

Lot No.:

Exp. Date:

Warning:

Do not administer in diseases where high potassium levels may be encountered, such as severe renal insufficiency or adrenal insufficiency.

​Indication:

For use as a supplement in potassium deficient states in cats and dogs.

Storage:

​Store tightly closed container in a dry place at a temperature not exceeding 35°C (95°F).

SPL UNCLASSIFIED SECTION

Distributed by: MWI

Boise, ID 83705

(888) 694-8381

www.VetOne.net

Rev. 07/13

PRINCIPAL DISPLAY PANEL - 4 oz Bottle

NDC: 13985-591-51

RenaPlus™

Potassium Gluconate

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

VETone®

V 502060
Net Contents: 4 oz (113 g)

For use in animals only.

Keep out of reach of children.

INGREDIENTS AND APPEARANCE

RENAPLUS 
potassium gluconate powder

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 13985-591
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

Inactive Ingredients
Ingredient Name	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Product Characteristics
Color	brown	Score
Shape		Size
Flavor	LIVER	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 13985-591-51	113 g in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/06/2014

Labeler - MWI/VetOne (019926120)

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