Rumatel

Dosage Form: FOR ANIMAL USE ONLY
Rumatel® 88

(morantel tartrate)

TYPE A MEDICATED ARTICLE

For cattle and goats

Active Drug Ingredient:

Morantel tartrate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19.4% (88 g/lb)

Indications for Use:

Cattle: For the removal and control of mature gastrointestinal nematode infections of cattle including stomach worms (Haemonchus spp., Ostertagia spp., Trichostrongylus spp.), worms of the small intestine (Cooperia spp., Trichostrongylus spp., Nematodirus spp.), and worms of the large intestine (Oesophagostomum radiatum). 

Goats: For the removal and control of mature gastrointestinal nematode infections of goats including Haemonchus contortus, Ostertagia (Teladorsagia) circumcincta, and Trichostrongylusaxei.

CAUTION:

For use in the manufacture of medicated beef, dairy, and goat feeds.

CAUTION: Certain components of animal feeds, including medicated premixes, possess properties that may be a potential health hazard or a source of personal discomfort to certain individuals who are exposed to them. Human exposure should, therefore, be minimized by observing the general industry standards for occupational health and safety.

Precautions such as the following should be considered: dust masks or respirators and protective clothing should be worn; dust-arresting equipment and adequate ventilation should be utilized; personal hygiene should be observed; wash before eating or leaving a work site; be alert for signs of allergic reactions–seek prompt medical treatment if such reactions are suspected.

STORE IN A DRY, COOL PLACE

Mixing and Use Directions

The following are examples in the approved range (0.44–4.4 g/lb)

lb of feed per 100 lb of body weight	lb of premix	lb of nonmedicated feed	Resulting concentration (g/lb)
1.0	10	1990	0.44
0.4	25	1975	1.10
0.2	50	1950	2.20
0.1	100	1900	4.40

Directions for Use of Medicated Ration

Use a single therapeutic treatment. Medicated feed is to be fed at the rate of 0.44 grams of morantel tartrate per 100 lb of body weight. The medicated feed mix should be consumed within 6 hours. May be fed as the sole ration or mixed with 1–2 parts of complete feed or as a top dress. When used as a top dress the medication as well as the underlying feed should be evenly distributed. Animals should be grouped by size for optimum efficacy. Fresh water should be available at all times. When all medicated feed is consumed resume normal feeding. Conditions of constant worm exposure may require retreatment within 2–4 weeks. Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism.

WARNINGS:

Do not treat cattle within 14 days of slaughter.

Do not treat goats within 30 days of slaughter. No milk

discard required following use in dairy cattle or goats.

CAUTION: Consult veterinarian before using in severely debilitated animals. Do not mix in feeds containing bentonite.

SEE BACK PANEL FOR FURTHER USE DIRECTIONS

Net Weight: 25 lb (11.3 kg)

NADA #92-444, Approved by FDA

7968000

101-9016-02

Made in USA

Rumatel 88  morantel tartrate  powder

Product Information Product Type OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG NDC Product Code (Source) 66104-2400 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MORANTEL TARTRATE (MORANTEL) MORANTEL TARTRATE 88 g  in 0.45 kg

Inactive Ingredients Ingredient Name Strength MINERAL OIL   SODIUM ALUMINIUM SILICATE   CALCIUM CARBONATE   SOYBEAN

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 66104-2400-5 11.3 kg In 1 BAG None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NADA	NADA92444	03/25/2010

Labeler - Phibro Animal Health (006989008)

Revised: 04/2010Phibro Animal Health