Label: RENACARE K- potassium gluconate gel

  • NDC Code(s): 52261-7001-1
  • Packager: Cosco International, Inc.
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated May 1, 2024

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  • Product Facts

    Potassium Gluconate ............2 mEq (468 mg) per 2.5g

  • INACTIVE INGREDIENTS:

    Biotin, Citric Acid, Cyanocobalamin, Folic Acid, Maple Flavor, Niacinamide, Pantothenic Acid, Potassium Sorbate, Purified Water, Pyridoxine Hydrochloride, Riboflavin, Sodium Benzoate, Sodium Carboxymethylcellulose, Sucralose, Thiamine Hydrochloride.

  • CAUTIONS:

    If animal's condition worsens or does not improve, stop product administration and consult your veterinarian.

    Safe use in pregnant animals or animals intended for breeding has not been proven.

    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 U.S.A

    Distributed by:

    Pet Health Pharma, Inc.

    7726 N First St. Suite 272

    Fresno, CA 93720

    559-900-7038

    pethealthpharma.com

  • PRINCIPAL DISPLAY PANEL

    5oz label

  • INGREDIENTS AND APPEARANCE
    RENACARE K 
    potassium gluconate gel
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:52261-7001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Potassium Gluconate (UNII: 12H3K5QKN9) (POTASSIUM CATION - UNII:295O53K152) Potassium Gluconate468 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    BIOTIN (UNII: 6SO6U10H04)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    CYANOCOBALAMIN (UNII: P6YC3EG204)  
    FOLIC ACID (UNII: 935E97BOY8)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PANTOTHENIC ACID (UNII: 19F5HK2737)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    WATER (UNII: 059QF0KO0R)  
    PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)  
    RIBOFLAVIN (UNII: TLM2976OFR)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    THIAMINE HYDROCHLORIDE (UNII: M572600E5P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52261-7001-1142 g in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/01/2024
    Labeler - Cosco International, Inc. (016433141)
    Registrant - Cosco International, Inc. (016433141)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosco International, Inc.016433141manufacture, api manufacture
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