Renal K Plus

Manufacturer
Vetoquinol USA, Inc. | Vetoquinol N.-A. INC
Effective date
2020-02-19
Label type
OTC ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:40:43

Label at a glance#

ProductRenal K Plus
Active ingredientPotassium Gluconate
Label structure9 sections

Dosage and administration

For Adult Dogs and Cats:   1 level scoop per 10 lbs. (4.5 kg) of body weight.   Give orally twice daily. Administer at mealtime. Adjust amount based on veterinary recommendations.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Product Facts

DESCRIPTION SECTION

ACTIVE INGREDIENTS PER 1 LEVEL SCOOP INCLUDED (2.2mEq):

Potassium Gluconate2.2mEq (514 mg)

INACTIVE INGREDIENTS:

SPL UNCLASSIFIED SECTION

Brewer's Dried Yeast, Hydrolyzed Fish (enzymatic), Hydrolyzed Poultry Liver (enzymatic), Mixed Tocopherols (a preservative), Sodium Acid Pyrophosphate, Sodium Sulfate.

CAUTIONS:

PRECAUTIONS SECTION

Safe use in pregnant animals or animals intended for breeding has not been proven. If animal's condition worsens or does not improve, stop product administration and consult your veterinarian. Administer during or after the animal has eaten to reduce incidence of gastrointestinal upset. Do not administer to cats or dogs with acute, oliguric, anuric or very advanced renal failure. Do not administer in other diseases where high potassium levels may occur, such as adrenal insufficiency, acute dehydration or urethral obstruction. Use with caution in the presence of cardiac disease, particularly in digitalized patients.

INTENDED USE:

VETERINARY INDICATIONS SECTION

For use in adult dogs or cats only.

Recommended for Renal Health Support.

Renal K+™ is a supplement for cats and dogs in a potassium deficient state. Each 530 mg (1 level scoop) contains 2.2mEq of potassium (as potassium gluconate) in a palatable base.

DIRECTIONS FOR USE:

DOSAGE & ADMINISTRATION SECTION

SPL UNCLASSIFIED SECTION

For Adult Dogs and Cats:

  • 1 level scoop per 10 lbs. (4.5 kg) of body weight.
  • Give orally twice daily.

Administer at mealtime. Adjust amount based on veterinary recommendations.

WARNINGS:

WARNINGS SECTION

FOR ANIMAL USE ONLY. KEEP OUT OF REACH OF CHILDREN AND ANIMALS. IN CASE OF ACCIDENTAL OVERDOSE, CONTACT A HEALTH PROFESSIONAL IMMEDIATELY. STORE IN A COOL, DRY PLACE.

QUESTIONS?

SPL UNCLASSIFIED SECTION

Made in Canada by Vetoquinol N.-A. Inc.
Princeville, Quebec, Canada
Distributed by Vetoquinol USA, Inc.
Ft. Worth, TX (USA) 76137
1 (800) 267-5707
www.vetoquinolusa.com

410631
13
993227J

PRINCIPAL DISPLAY PANEL - 100 g Container Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 17030-082-10

Renal K+™
(Potassium Gluconate)

Potassium Supplement ▶
To Support Renal Health ▶
For Dogs & Cats ▶

ORAL POWDER

QUALITY SEAL
nasc
NATIONAL ANIMAL SUPPLEMENT COUNCIL

Net Contents: 3.53 oz (100g)

(Approx. 188 level scoops)

vetoquinol

PRINCIPAL DISPLAY PANEL - 100 g Container Label
PRINCIPAL DISPLAY PANEL - 100 g Container Label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
POTASSIUM CATION Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17030-082-10Renal K Plus100 g in 1 CONTAINERPOWDER1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17030-082RENAL K PLUS (POTASSIUM GLUCONATE) POWDER [VETOQUINOL USA, INC.]11 package rows20200220_4f8b6a7f-1a8e-499d-a91b-7f5624dc18b0.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17030-08217030-082-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.