Label: IVERMECTIN- ivermectin oral paste
- NDC Code(s): 86213-771-01
- Packager: Vetr LLC
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated May 14, 2025
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- Animal Safety
- SPL UNCLASSIFIED SECTION
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Directions for Use
One syringe contains sufficient paste to treat one 1250 lb horse at the recommended dose rate (0.2 mg/kg) body weight. 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.
- Storage
- Active Ingredients
- Other Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
IVERMECTIN
ivermectin oral pasteProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:86213-771 Route of Administration Oral Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IVERMECTIN (UNII: 8883YP2R6D) (IVERMECTIN - UNII:8883YP2R6D) IVERMECTIN 18.7 mg in 1 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) Product Characteristics Color white (off white to yellow-white) Score Shape Size Flavor APPLE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:86213-771-01 6.1 g in 1 SYRINGE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/07/2025 Labeler - Vetr LLC (132219984) Establishment Name Address ID/FEI Business Operations Vetr LLC 132219984 manufacture, label