DESCRIPTION SECTION
RenaKare™
Potassium Gluconate Powder
CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.
RenaKare
- Manufacturer
- Neogen Corporation-Mercer Rd | Jungbunzlauer Ladenburg GmbH
- Effective date
- 2023-02-21
- Label type
- PRESCRIPTION ANIMAL DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 02:41:53
Label at a glance#
ProductRenaKare
Active ingredientPOTASSIUM GLUCONATE
Label structure8 sections
Label contents#
Full prescribing information#
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.
SPL UNCLASSIFIED SECTION
Item No. 09075
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
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| POTASSIUM CATION Pharmacologic Class Indexing | 3 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59051-9075-1 | RenaKare | 113 g in 1 BOTTLE, PLASTIC | POWDER | 113 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 59051-9075 | RENAKARE (POTASSIUM GLUCONATE) POWDER [NEOGEN CORPORATION-MERCER RD] | 3 | 1 package rows | 20230222_af6cbe7b-bdb7-49c5-9ec1-ac3942889366.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| POTASSIUM GLUCONATE | ACTIVE INGREDIENT | 12H3K5QKN9 | 1 | |
| POTASSIUM CATION | ACTIVE MOIETY | 295O53K152 | 1 |
Products#
Every source-derived product name is available through these pages.
- RenaKare
- Potassium Gluconate
- POTASSIUM CATION
- PORK LIVER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 59051-9075 | 59051-9075-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| POTASSIUM GLUCONATE | 12H3K5QKN9 | ACTIB |
| PORK LIVER | 6EC706HI7F | IACT |
Source Document#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.