Label: RENAL K PLUS- potassium gluconate gel
- NDC Code(s): 17030-081-05
- Packager: Vetoquinol USA, Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 13, 2020
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- Official Label (Printer Friendly)
- VETERINARY INDICATIONS
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENTS PER ½ TSP (2.5 mL):
- INACTIVE INGREDIENTS:
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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:
- DIRECTIONS FOR USE:
- WARNINGS:
- QUESTIONS?
- PRINCIPAL DISPLAY PANEL - 142 g Tube Label
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INGREDIENTS AND APPEARANCE
RENAL K PLUS
potassium gluconate gelProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:17030-081 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Potassium Gluconate (UNII: 12H3K5QKN9) (POTASSIUM CATION - UNII:295O53K152) Potassium Gluconate 187.2 mg in 2.5 g Inactive Ingredients Ingredient Name Strength 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 Color BROWN (Translucent, golden paste) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17030-081-05 142 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 06/17/2019 Labeler - Vetoquinol USA, Inc. (106824209) Establishment Name Address ID/FEI Business Operations Vetoquinol N.-A. INC 202919940 API MANUFACTURE, MANUFACTURE, LABEL