TOLTRAMAX POWDER 5% (5% toltrazuril powder- 50 mg/g powder TOLTRAMAX POWDER 5% (5% toltrazuril powder- 50mg/g powder

Toltramax Powder 5% by

Drug Labeling and Warnings

Toltramax Powder 5% by is a Animal medication manufactured, distributed, or labeled by Vetr, LLC, Alivira Animal Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS AND PRECAUTIONS

Keep out of reach of children. Recognized as safe for use in pregnant and lactating females and puppies & kittens over four weeks of age.

DOSAGE & ADMINISTRATION

Shake/mix well before use. Dose at 1 g of powder (50 mg toltrazuril) per 5 pounds of body weight, for 3-5 consecutive days. Toltramax should be administered orally and retreatment may be necessary after 4-6 weeks.   

STORAGE AND HANDLING

Store at room temperature (at or below 77F).

ACTIVE INGREDIENT

Toltrazuril USP, 5% w/w (50 mg/g)

INACTIVE INGREDIENT

Maltodextrin, silicon dioxide, natural and artificial flavor

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TOLTRAMAX POWDER 5% 
5% toltrazuril powder (50 mg/g) powder

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 86213-141
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLTRAZURIL (UNII: QVZ3IAR3JS) (TOLTRAZURIL - UNII:QVZ3IAR3JS)	TOLTRAZURIL	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Product Characteristics
Color	white	Score
Shape		Size
Flavor	MEAT (BEEF Flavored)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 86213-141-01	100 g in 1 JAR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/12/2025

TOLTRAMAX POWDER 5% 
5% toltrazuril powder (50 mg/g) powder

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 86213-142
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLTRAZURIL (UNII: QVZ3IAR3JS) (TOLTRAZURIL - UNII:QVZ3IAR3JS)	TOLTRAZURIL	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Product Characteristics
Color	white	Score
Shape		Size
Flavor	CHICKEN	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 86213-142-01	100 g in 1 JAR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/12/2025

TOLTRAMAX POWDER 5% 
5% toltrazuril powder (50mg/g) powder

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 86213-143
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLTRAZURIL (UNII: QVZ3IAR3JS) (TOLTRAZURIL - UNII:QVZ3IAR3JS)	TOLTRAZURIL	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Product Characteristics
Color	white	Score
Shape		Size
Flavor	CINNAMON	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 86213-143-01	100 g in 1 JAR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/12/2025

Labeler - Vetr, LLC (132219984)

Establishment
Name	Address	ID/FEI	Business Operations
Vetr, LLC		132219984	manufacture, label

Establishment
Name	Address	ID/FEI	Business Operations
Alivira Animal Health		650916617	api manufacture