OVUGEL- triptorelin acetate gel

OvuGel by

Drug Labeling and Warnings

OvuGel by is a Animal medication manufactured, distributed, or labeled by Aurora Pharmaceutical, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT:

triptorelin acetate

DOSAGE FORM & STRENGTH:

100 mcg triptorelin per mL (as triptorelin acetate)
Gel for intravaginal use

INDICATIONS FOR USE:

For the synchronization of time of insemination in weaned sows to facilitate a single fixed-time artificial insemination.  Not approved for use in gilts.  Safety and effectiveness have not been evaluated in these animals.

DESCRIPTION:

OvuGel® is a thin, clear to slightly hazy gel.  Each mL of OvuGel® contains 100 mcg of triptorelin (as triptorelin acetate) for intravaginal administration.

WARNINGS:

WITHDRAWAL PERIOD:

No withdrawal period is required when used according to labeling.

USER SAFETY WARNINGS:

Not for Use in Humans.  Keep Out of Reach of Children.  The Material Safety Data Sheet (MSDS) contains more detailed occupational safety information.

ANIMAL SAFETY WARNINGS:

OvuGel® should not be used in sows with obvious reproductive tract abnormalities.

RECOMMENDATIONS FOR SAFE AND EFFECTIVE USE:

Use of a bottle mount multi-dose applicator is recommended to ensure accurate dosing.
The use of adequate sperm numbers per insemination and proper semen storage, as recommended by the semen or artificial inseminator catheter suppliers, is recommended.

DIRECTIONS FOR USE:

OvuGel® should be administered intravaginally at approximately 96 hours after weaning.  The product should be warmed at room temperature for a minimum of 10 minutes prior to use.  Insert the delivery tube into the vagina so that the tip rests 1/2 inch (1-3 cm) posterior to the cervix.  Use a separate sheath over the delivery tube for each sow treated.  Each sow should receive a single 2 mL dose of OvuGel®.  Sows should be inseminated 22 +/- 2 hours following administration of OvuGel® using standard artificial insemination techniques.  Sows should be exposed to a boar during time of insemination.  (See end of package insert for more detailed directions for OvuGel® administration).

STORAGE, HANDLING, AND DISPOSAL:

Store at refrigerator temperature 36-46°F (2-8°C).  Excursions permitted to 77°F (25°C) for no more than 5 days during shipping.
OvuGel® should be administered within 1 hour of warming; unused portions may be refrigerated immediately after use.  The bottle stopper may be punctured a maximum of three times.  Discard 28 days after the stopper is first punctured.

HOW SUPPLIED:

OvuGel® is available in 52.5 mL multi-dose bottle.

QUESTIONS/COMMENTS

To obtain an MSDS, for technical assistance, or to report adverse events, contact Aurora Pharmaceutical at 1-888-215-1256 or www.aurorapharmaceutical.com. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS, or www.fda.gov/reportanimalae.

SPL UNCLASSIFIED SECTION

Approved by FDA under NADA #141-339
NDC: 51072-087-00

PRINCIPAL DISPLAY PANEL

Principal Display Panel – 52.5 mL Bottle Carton
OvuGel®
(triptorelin acetate)
100 mcg triptorelin per mL (as triptorelin acetate)
Gel for intravaginal use

INDICATIONS FOR USE:
For the synchronization of time of insemination in weaned sows to facilitate a single fixed-time artificial insemination.

Not approved for use in gilts. Safety and effectiveness have not been evaluated in these animals.

Net Contents: 52.5 mL
multi-dose bottle (26 doses, 2 mL each)

Approved by FDA under NADA # 141-339
NDC: 51072-087-00

Manufactured by: Aurora Pharmaceutical, Inc.
1196 Hwy 3 S
Northfield, MN 55057

IN 40-1859 Rev. 02/2025
Reorder No: 59030

INGREDIENTS AND APPEARANCE

OVUGEL 
triptorelin acetate gel

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 51072-087
Route of Administration	VAGINAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Triptorelin Acetate (UNII: 43OFW291R9) (Triptorelin - UNII:9081Y98W2V)	Triptorelin	100 ug  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51072-087-00	1 in 1 CARTON
1		52.5 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NADA	NADA141339	01/20/2026

Labeler - Aurora Pharmaceutical, Inc. (832848639)

Establishment
Name	Address	ID/FEI	Business Operations
Aurora Pharmaceutical, Inc.		832848639	manufacture