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Merck Animal Health

Ralgro Cattle Implants

Ralgro Cattle Implants

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Ralgro implant contains zeranol, an anabolic agent which stimulates weight gain and feed efficiency in cattle. Each dose contains 36 mg (3 pellets) of Zeranol. Approved for implanting suckling calves. growing beef cattle. feedlot steers and heifers and replacement heifers between 1 month of age and weaning. Not cleared for use in heifers or bulls that will be used for breeding stock, lactating animals, or veal calves. Packaged in cartridges containing 24 doses.

For increased rate of weight gain and for improved feed conversion of weaned beef calves, growing beef cattle, feedlot steers and feedlot heifers. For increased rate of weight gain of suckling beef calves. Can increase weaning weight by as much as 20-35 lbs in calves. Each dose contains 36 mg zeranol. Do not implant bulls intended for reproduction, veal calves or dairy animals. Do not use before 1 month of age or after weaning in heifers intended for reproduction. Ralogun Applicator and Replacement Ralogun Needles sold separately. For use in beef steers and heifers, including replacements. Do not use before 1 month of age or after weaning in heifers intended for reproduction. NOT for human use.

Dosage: one dose implanted SQ on the backside of the ear.

Size: 24 dose cartridge 

Manufacturer and/or Label Information

MERCK ANIMAL HEALTH
Intervet Inc.
2 GIRALDA FARMS, MADISON, NJ, 07940
Customer Service: 800-521-5767
Order Desk: 800-648-2118
Technical Service (Companion Animal): 800-224-5318
Technical Service (Livestock): 800-211-3573
Fax: 973-937-5557
Website: www.merck-animal-health-usa.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.
RALGRO® IMPLANTS FOR BEEF CATTLE

Intervet/Merck Animal Health

(zeranol implants)

IMPLANTS IN CARTRIDGES for Beef Cattle

CAUTION: Do not use in bulls intended for reproduction or dairy animals. Do not use before 1 month of age or after weaning in heifers intended for reproduction. Edema of the vulva and udder, teat elongation, rectal and vaginal prolapse, and signs of estrus may occur when heifers are implanted. Delayed testicular development may occur in young males. To avoid difficulty in castration, young males should be castrated at the time of implanting.

Dosage: 36 mg zeranol

A single pull of the RALOGUN® trigger delivers the proper 36-mg dose (three - 12-mg pellets per chamber). Manufactured by a non-sterilizing process.

Restricted Drug (California), Use Only as Directed.


WARNING:

DO NOT ATTEMPT TO SALVAGE IMPLANT SITE FOR HUMAN OR ANIMAL FOOD. IMPLANT PELLETS IN THE EAR ONLY. ANY OTHER LOCATION IS IN VIOLATION OF FEDERAL LAW. A WITHDRAWAL PERIOD HAS NOT BEEN ESTABLISHED FOR THIS PRODUCT IN PRE-RUMINATING CALVES. DO NOT USE IN CALVES TO BE PROCESSED FOR VEAL.


DIRECTIONS FOR USING RALGRO® (zeranol implants) IN CARTRIDGES WITH THE RALOGUN® PELLET INJECTOR

RALGRO (zeranol implants) is an anabolic agent that increases rate of weight gain and improves feed efficiency of weaned beef calves, growing beef cattle, feedlot steers, and feedlot heifers. RALGRO also increases rate of weight gain of suckling beef calves. Do not use in veal calves.

Effectiveness and animal safety in veal calves have not been established. RALGRO pellets are stable when stored between 2° and 25° C (36° and 77°F). RALGRO pellets each contain 12 mg of zeranol. Three pellets are required for 36-mg dose.

STEP 1


Each chamber of the plastic RALGRO cartridge contains a full dose of RALGRO implants. Insert the cartridge in the magazine of the RALOGUN pellet injector with the hole in the axle of the cartridge pointed toward the handle of the RALOGUN pellet injector. After snapping into place, rotate cartridge clockwise to ensure proper seating, then check window at top to ensure that pellet chamber is aligned with plunger.

STEP 2


Always use sharp needle. A dull needle tears tissue and makes proper implanting difficult. Be sure that needle is fully seated in RALOGUN pellet injector. This ensures that pellets will be expelled from the needle as RALOGUN plunger is extended. Failure to set the needle could cause the last pellet to be left in the needle and not implanted.

STEP 3


After appropriately restraining the animal to allow access to the ear, cleanse the skin at the implant needle puncture site.

STEP 4


The implant site is subcutaneous, between the skin and cartilage on the back side of the ear and below the midline of the ear. The implant must not be placed closer to the head than the edge of the auricular cartilage ring farthest from the head. The location for insertion of the needle is a point toward the tip of the ear and at least a needle length away from the intended deposition site. Care should be taken to avoid injuring the major blood vessels or cartilage of the ear. Squeeze trigger of the RALOGUN pellet injector to deliver a full dose of RALGRO. Keep trigger depressed while withdrawing the needle to be sure that RALGRO implants stay in place.

STEP 5


Wipe needle with cotton or gauze moistened with alcohol or other suitable disinfectant. Do not dip needle in solution because solution clinging to inside of needle will cause plugging of needle.

STEP 6


Rotate cartridge in direction of arrow until a new dose is visible and centered in window. The RALOGUN pellet injector is now ready for next implantation.

Made in Austria

This product may not be marketed or used in the EU.

Approved by FDA under NADA # 038-233

Distributed by: Intervet Inc d/b/a Merck Animal Health, Madison, NJ 07940

Copyright © 2022 Merck & Co., Inc., Rahway, NJ, USA and its affiliates. All rights reserved.

999633 R3



NDC



1 cartridge of 24 doses

0061-5026-02

352858 R2

Ten 24-dose cartridges
240 doses (24 doses per cartridge)

0061-5026-03

999367 R2

CPN: 1047168.5

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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