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Zoetis

Valbazen Suspension Broad Spectrum Dewormer

Valbazen Suspension Broad Spectrum Dewormer

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Broad-spectrum anthelmintic for oral administration, effective in the removal and control of liver flukes, stomach worms, tapeworms, intestinal worms and lungworms in cattle and sheep. Also, for treatment of adult liver flukes in non-lactating goats.

Contains 113.6 mg albendazole per ml.

Administer orally.

Dosage: Cattle - 4 ml per 100 lbs body wt; Sheep - 0.75 ml per 25 lbs body wt; Goats - 4 ml per 100 lbs body wt. Do not use in female dairy cattle of breeding age or lactating does.

Do not administer to female cattle during the first 45 days of pregnancy or for 45 days after removal of bulls. Do not administer to ewes during the first 30 days of pregnancy or for 30 days after removal of rams.

Slaughter withdrawal: Cattle - 27 days; Sheep and Goats - 7 days.

Item cannot be shipped to California. 


Manufacturer and/or Label Information

ZOETIS INC.
333 PORTAGE STREET, KALAMAZOO, MI, 49007
Telephone: 269-359-4414
Customer Service: 888-963-8471
Website: www.zoetis.com
THIS SERVICE AND DATA ARE PROVIDED "AS IS". DVMetrics assumes no liability, and each user assumes full risk, responsibility, and liability, related to its use of the DVMetrics service and data. See the Terms of Use for further details.
VALBAZEN®

Zoetis

(albendazole oral suspension)

Broad-Spectrum Dewormer

Oral Suspension for Use in Cattle, Sheep, and Goats for removal and control of liver flukes, tapeworms, stomach worms (including 4th stage inhibited larvae of Ostertagia ostertagi), intestinal worms, and lungworms in cattle and sheep and for the treatment of adult liver flukes in nonlactating goats

Active Ingredient:

Albendazole

11.36%

(Equivalent to 113.6 mg/mL)

Approved by FDA under NADA # 110-048

Indications:

Cattle and sheep: Valbazen is a broad-spectrum anthelmintic effective in the removal and control of liver flukes, tapeworms, stomach worms (including 4th stage inhibited larvae of Ostertagia ostertagi), intestinal worms, and lungworms as indicated below.

Goats: For the treatment of adult liver flukes in nonlactating goats.

Parasite

Cattle

Sheep

Goats

Adult Liver Flukes

Fasciola hepatica

Fasciola hepatica, Fascioloides magna

Fasciola hepatica

Heads and Segments of Tapeworms

Moniezia benedeni, M. expansa

Common Tapeworm (Moniezia expansa), Fringed Tapeworm (Thysanosoma actinioides)



Adult and 4th Stage Larvae of Stomach Worms

Brown Stomach Worm, including 4th stage inhibited larvae (Ostertagia ostertagi), Barber Pole Worm (Haemonchus contortus, H. placei), Small Stomach Worm (Trichostrongylus axei)

Brown Stomach Worm (Ostertagia circumcincta, Marshallagia marshalli), Barber Pole Worm (Haemonchus contortus), Small Stomach Worm (Trichostrongylus axei)



Adult and 4th Stage Larvae of Intestinal Worms

Thread-necked Intestinal Worm (Nematodirus spathiger, N. helvetianus), Small Intestinal Worm (Cooperia punctata, C. oncophora)

Thread-necked Intestinal Worm (Nematodirus spathiger, N. fificollis), Cooper’s Worms (Cooperia oncophora), Bankrupt Worm (Trichostrongylus colubriformis), Nodular Worm (Oesophagostomum columbianum), Large-mouth Bowel Worm (Chabertia ovina)



Adult Stages of Intestinal Worms

Hookworm (Bunostomum phlebotomum), Bankrupt Worm (Trichostrongylus colubriformis), Nodular Worm (Oesophagostomum radiatum)





Adult and 4th Stage Larvae of Lungworms

Dictyocaulus viviparus





Adult and Larval Stages of Lungworms



Dictyocaulus filaria



Dosage and Administration: Valbazen Suspension should be administered to cattle and goats at the recommended rate of 4 mL/100 lb of body weight (equivalent to 4.54 mg of albendazole/lb, 10 mg/kg) and to sheep at the recommended rate of 0.75 mL/25 lb of body weight (equivalent to 3.4 mg of albendazole/lb, 7.5 mg/kg). The following table indicates recommended dosing schedules. Do not underdose. Ensure each animal receives a complete dose based on a current body weight. Underdosing may result in ineffective treatment, and encourage the development of parasite resistance.

Cattle

Sheep

Goats

Body Weight

Dosage

Body Weight

Dosage

Body Weight

Dosage

250 lb

10 mL

25 lb

0.75 mL

25 lb

1 mL

500 lb

20 mL

50 lb

1.5 mL

50 lb

2 mL

750 lb

30 mL

75 lb

2.25 mL

75 lb

3 mL

1000 lb

40 mL

100 lb

3.0 mL

100 lb

4 mL

1250 lb

50 mL

200 lb

6.0 mL

200 lb

5 mL

1500 lb

60 mL

300 lb

9.0 mL

300 lb

6 mL

Cattle: 500 mL of Valbazen 11.36% Suspension will treat 25 animals weighing 500 lb. 1 liter of Valbazen 11.36% Suspension will treat 50 animals weighing 500 lb. 5 liters of Valbazen 11.36% Suspension will treat 250 animals weighing 500 lb.

Sheep: 500 mL of Valbazen 11.36% Suspension will treat 332 animals weighing 50 lb. 1 liter of Valbazen 11.36% Suspension will treat 664 animals weighing 50 lb. 5 liters of Valbazen 11.36% Suspension will treat 3320 animals weighing 50 lb.

Goats: 500 mL of Valbazen 11.36% Suspension will treat 250 animals weighing 50 lb. 1 liter of Valbazen 11.36% Suspension will treat 500 animals weighing 50 lb. 5 liters of Valbazen 11.36% Suspension will treat 2500 animals weighing 50 lb.

Valbazen 11.36% Suspension should be given orally using any type of standard dosing gun or dose syringe.

Important: Accurate estimates of the weight of the cattle, sheep, and goats to be treated are essential for most effective results with this product. Animals constantly exposed to internal parasites should be retreated as necessary.


Residue Warnings: Cattle must not be slaughtered within 27 days following last treatment. Sheep and Goats must not be slaughtered within 7 days following last treatment. Because a withdrawal time in milk has not been established, do not use in female dairy cattle of breeding age. Do not use in lactating does.


Other Warnings:

Parasite resistance may develop to any dewormer, and has been reported for most classes of dewormers. Treatment with a dewormer used in conjunction with parasite management practices appropriate to the geographic area and the animal(s) to be treated may slow the development of parasite resistance. Fecal examinations or other diagnostic tests and parasite management history should be used to determine if the product is appropriate for the herd/flock, prior to the use of any dewormer. Following the use of any dewormer, effectiveness of treatment should be monitored (for example, with the use of a fecal egg count reduction test or another appropriate method). A decrease in a drug’s effectiveness over time as calculated by fecal egg count reduction tests may indicate the development of resistance to the dewormer administered. Your parasite management plan should be adjusted accordingly based on regular monitoring.

Precaution: Do not administer to female cattle during first 45 days of pregnancy or for 45 days after removal of bulls. Do not administer to ewes or does during the first 30 days of pregnancy or for 30 days after removal of rams or bucks. Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism.

Keep This and All Medication Out of Reach of Children

Shake Well Before Using

For Use in Animals Only

Store at Controlled Room Temperature 20° - 25°C (68° - 77°F)

Protect From Freezing

Not for human use

Restricted Drug (California) - Use only as directed

Distributed by: Zoetis Inc., Kalamazoo, MI 49007

500 mL/16.9 fl oz (1 pt 1 fl oz)

40029174

1 L/33.8 fl oz (1 qt 1.8 fl oz)

40029175

5 L/169 fl oz (1 gal 1 qt 9 fl oz)

40029179

CPN: 3690030.5

COLORADO SERUM COMPANY4950 YORK STREET, P.O. BOX 16428, DENVER, CO, 80216-0428Telephone: 303-295-7527Order Desk: 800-525-2065Fax: 303-295-1923Website: www.colorado-serum.comEmail: colorado-serum@colorado-serum.comTHIS SERVICE AND DATA ARE PROVIDED "AS IS". DVMetrics assumes no liability, and each user assumes full risk, responsibility, and liability, related to its use of the DVMetrics service and data. See the Terms of Use for further details.

TETANUS TOXOID-CONCENTRATED

Colorado Serum

Adjuvanted

GENERAL INFORMATION: This product has been shown to be effective for the vaccination of healthy horses, cattle, sheep, goats, and swine against tetanus. This product was licensed prior to the requirement to establish a minimum age for use. The duration of immunity is unknown. For more information regarding efficacy and safety data, see productdata.aphis.usda.gov.

Safety in pregnant animals is unknown.

Tetanus Toxoid is prepared by detoxifying tetanus toxin in such a manner as to allow the antigenic properties to remain intact. Product is purified, concentrated and adjuvanted to provide a low dose effective immunizing agent.

Each serial is tested for purity, safety, and potency in accordance with USDA requirements.

Tetanus is caused by a neurotoxin produced by growth of Clostridium tetani, an anaerobic (lives without air) micro-organism, in necrotic tissue. Affected animals become stiff, have difficulty swallowing, and have an increased pulse rate. Breathing is labored. Spasmodic contractions of the muscular system occur, such as contracting muscles of the jaw.

Spasmodic contractions of the muscular system occur, such as contracting muscles of the jaw. Thus, the term “lockjaw” is often used. Legs and tail are often stiff with abdominal muscles contracted. Tetanus stricken animals may be unusually sensitive to light and heat. Temperature of the animal generally remains normal, elevating only shortly before death.

Protective antibody levels usually occur about two weeks after the second injection of the primary immunization series. In contrast, administration of Tetanus Antitoxin is recommended for immediate, emergency, passive treatment of exposed animals with unknown vaccination history or with signs of tetanus infection.

DIRECTIONS: Do not vaccinate within 21 days before slaughter. Store at 2-8° C. Do not freeze. Do not mix with other products. Shake well before use. Use entire contents when first opened.

PRECAUTIONS: A transitory local reaction may occur at injection site. Anaphylactoid reaction may occur following administration of products of this nature. If noted, administer adrenalin or equivalent. In case of human exposure, consult a physician.

DOSAGE & ADMINISTRATION: For primary immunization, two doses should be administered subcutaneously or intramuscularly approximately 30 days apart. Use intramuscularly for horses as local reactions are more likely to occur if injected subcutaneously.

Horses: 1 ml IM

Cattle: 1 ml SC or IM

Sheep, Goats, Swine: 0.5 ml SC or IM

Historically, annual single dose revaccination has been recommended. Contact veterinarian for advice.

OTHER INFORMATION: Contains thimerosal and formalin as preservatives. Tetanus Toxoid Concentrate is available in single dose size packaged 10 vials to the carton, and in 10 dose vials.

THE PEAK OF QUALITY SINCE 1923

VLN: 188 / PCN: 8601.00

COLORADO SERUM COMPANY, 4950 York Street, Denver, Colorado 80216

303-295-752

www.colorado-serum.com

Contact us for information on other Colorado Serum Company products. Fine Veterinary Products since 1923.

FOR VETERINARY USE ONLY

 

 

Order #

10 - 1 ml vials

10 - 1 dose vials

11411

10 ml

10 doses

11415

CPN: 1101033.3

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