Potassium

Indications

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

Dosage and Administration

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. Store in a dry place at a temperature between 15°-30°C (59°-86°F). Keep container tightly closed. UPC 7 26087 09076 4 ​KEEP OUT OF REACH OF CHILDREN

Warnings

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

Precautions

Use with caution in the presence of cardiac disease, particularly in digitalized patients or in the presence of renal disease. Manufactured for Neogen Corporation Lexington, KY 40511 859-254-1221 neogen.com 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) RenaKare Gel 5oz (142 g)

Other labels for this ingredient

These labels are also stored for the same active ingredient. They are not identical to the one reprinted above, and each is listed by product and set id rather than merged with it.

• RenaKare Potassium Gluconate POTASSIUM GLUCONATE POTASSIUM CATION, Neogen Corporation-Mercer. Set id 43642434-ed10-49da-954b-a6306cb939de.
• RenaPlus Potassium Gluconate POTASSIUM GLUCONATE POTASSIUM CATION SILICON DIOXIDE, MWI/VetOne. Set id 90caffe1-92bc-4c8d-baee-486611a9cffa.
• RenaPlus Potassium Gluconate POTASSIUM GLUCONATE POTASSIUM CATION, MWI/VetOne. Set id 10e2e633-9bc5-41d7-89ab-a10a928e89ce.

FDA adverse event reports

The FDA Center for Veterinary Medicine publishes the adverse event reports it receives through openFDA. The counts below are the reports naming potassium as an active ingredient for each species this label names, as returned on 2026-09-16, coded by the VeDDRA reaction term the reporter chose. Reactions are counted per report, so one report can appear under several terms.

These are counts, not rates. Reporting is voluntary, the number of animals treated is not known, and a widely used product accumulates reports for that reason alone. A report records that an event followed a dose; it does not establish that the product caused it. The counts say nothing about how one product compares with another.