Label: RENAL K PLUS- potassium gluconate gel

  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated February 13, 2020

If you are a consumer or patient please visit this version.

  • VETERINARY INDICATIONS

    Renal K+™ is a supplement for adult cats and dogs in a potassium deficient state.

  • SPL UNCLASSIFIED SECTION

    Product Facts

  • ACTIVE INGREDIENTS PER ½ TSP (2.5 mL):

    Potassium Gluconate2 mEq (468 mg)
  • INACTIVE INGREDIENTS:

    Biotin, Calcium D Pantothenate, Citric Acid, Cyanocobalamin, Folic Acid, Maple Flavor, Niacinamide, Potassium Sorbate, Purified Water, Pyridoxine Hydrochloride, Riboflavin 5'-Sodium Phosphate, Sodium Benzoate, Sodium Carboxymethylcellulose, Sucralose, Thiamine Hydrochloride.

  • CAUTIONS:

    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.

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

    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 be encountered, such as adrenal insufficiency, acute dehydration or urethral obstruction.

  • INTENDED USE:

    FOR USE IN ADULT CATS & DOGS ONLY

    Recommended for Renal Health Support

  • DIRECTIONS FOR USE:

    Administer orally: Adult dogs and cats give 1/2 teaspoon per 10 lbs. (4.5 kg) body weight, twice daily. Adjust amount based on veterinary recommendations.

  • WARNINGS:

    FOR ANIMAL USE ONLY. KEEP OUT OF THE REACH OF CHILDREN AND ANIMALS. IN CASE OF ACCIDENTAL OVERDOSE, CONTACT A HEALTH PROFESSIONAL IMMEDIATELY. STORE AT A CONTROLLED ROOM TEMPERATURE.

  • QUESTIONS?

    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

    Lot No & Exp. Date on Crimp of Tube

  • PRINCIPAL DISPLAY PANEL - 142 g Tube Label

    NDC 17030-081-05

    Renal K+™
    (Potassium Gluconate)

    Potassium
    Supplement ▶

    To Support
    Renal Health ▶

    Palatable ▶

    For Dogs & Cats ▶

    ORAL GEL

    Net Contents: 5oz (142g)

    QUALITY SEAL
    nasc
    NATIONAL ANIMAL SUPPLEMENT COUNCIL

    vetoquinol

    PRINCIPAL DISPLAY PANEL - 142 g Tube Label
  • INGREDIENTS AND APPEARANCE
    RENAL K PLUS 
    potassium gluconate gel
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:17030-081
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Potassium Gluconate (UNII: 12H3K5QKN9) (POTASSIUM CATION - UNII:295O53K152) Potassium Gluconate187.2 mg  in 2.5 g
    Inactive Ingredients
    Ingredient NameStrength
    BIOTIN (UNII: 6SO6U10H04)  
    CALCIUM PANTOTHENATE (UNII: 568ET80C3D)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    CYANOCOBALAMIN (UNII: P6YC3EG204)  
    FOLIC ACID (UNII: 935E97BOY8)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    WATER (UNII: 059QF0KO0R)  
    PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)  
    RIBOFLAVIN 5'-PHOSPHATE SODIUM ANHYDROUS (UNII: 957E53WV42)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    THIAMINE HYDROCHLORIDE (UNII: M572600E5P)  
    Product Characteristics
    ColorBROWN (Translucent, golden paste) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17030-081-05142 g in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    UNAPPROVED DRUG OTHER06/17/2019
    Labeler - Vetoquinol USA, Inc. (106824209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vetoquinol N.-A. INC202919940API MANUFACTURE, MANUFACTURE, LABEL