TUMIL-K- potassium gluconate powder 
Virbac AH, Inc.

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.

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Tumil-K Powder

DOSAGE: The suggessted dose of TUMIL-K for adult cats and dogs is 0.65 g (1/4 level teaspoonful) per 10 lb (4.5 kg) body weight twice daily with food.  Dosage may be adjusted to satisfy patient's need. 

INDICATION:

For use as a supplement in potassium deficient states in cats and dogs.  

WARNINGS:

Do not administer to cats 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, urethral obstruction.  

PRECAUTION:

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

CAUTION:

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

KEEP THIS AND ALL MEDICATIONS OUT OF THEREACH OF CHILDREN.

STORE AT CONTROLLED ROOM TEMPERATURE15°-30°C (59°-86°F).

Mfg. for: Virbac AH, Inc. • P.O. Box 162059 Fort Worth, TX 76161 • (800) 338-3659

Front Panel Display --4 oz Bottle

NDC 051311-846-04

TUMIL-K®

Each 0.65 g (1/4 level teaspoonful) contains: Potassium Gluconate 2mEq (468 mg) in a palatable protein base.

INDICATION: For use as a supplement in potassium deficient states in cats and dogs.

4 oz

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Virbac 

Animal Health

Mfg. for: Virbac AH, Inc. • P.O. Box 162059 Fort Worth, TX 76161 • (800) 338-3659

image description

TUMIL-K 
potassium gluconate powder
Product Information
Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:51311-846
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM GLUCONATE (UNII: 12H3K5QKN9) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM GLUCONATE2 meq  in 0.65 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51311-846-04113.3 g in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/01/200407/31/2017
Labeler - Virbac AH, Inc. (131568396)
Registrant - Virbac AH, Inc. (131568396)
Establishment
NameAddressID/FEIBusiness Operations
Virbac Corporation829166276manufacture
Establishment
NameAddressID/FEIBusiness Operations
Purac Biochem B.V.405232687api manufacture

Revised: 4/2017
Document Id: 56c09cd5-df4d-4e60-ba72-b134e4096101
Set id: 9222e295-95a9-42c2-9963-1cde3ed185d3
Version: 2
Effective Time: 20170403
 
Virbac AH, Inc.