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Terconazole: Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx)
Strength:
8 mg/g
Drug class:
Active ingredient:

Patient information: uses, side effects, how to take - Terconazole

INSTRUCTIONS FOR USE

Instructions for Use

TERCONAZOLE VAGINAL CREAM (ter kon ah zol)

For vaginal use only. Do not put Terconazole vaginal cream in your eyes or mouth.

Be sure to read, understand, and follow the instructions below for how to use Terconazole vaginal cream, correctly.

Important Information

  • Use Terconazole vaginal cream exactly as your healthcare provider tells you to use it.
  • Use1 full applicator of terconazole vaginal cream in the vagina each night at bedtime for 3 days in a row.
  • Do not stop using Terconazole vaginal cream before your healthcare provider tells you to, even if you feel better very quickly. Your infection may not clear up completely.
  • If you have questions or if your vaginal symptoms do not go away, contact your healthcare provider.

How should I store terconazole vaginal cream?

  • Store Terconazole vaginal cream at room temperature between 68°F to 77°F (20°C to 25°C).

Keep Terconazole vaginal cream and all medicines out of the reach of children.

  • Step 1. Gather your supplies. (Figure 1)
  • 1 Terconazole vaginal cream tube
  • 1 empty reusable applicator, to fill and give the dose of medicine.
Step 2. Wash your hands.

Step 3. Prepare the Applicator:

  • Remove the cap from the Terconazole vaginal cream tube.
  • Use the pointed tip on the top of the cap to puncture the seal on the tube. (See Figure 2)
  • Screw the applicator onto the tube.
  • Squeeze the tube from the bottom and fill the applicator until the plunger stops. (See Figure 3)
  • Unscrew the applicator from the tube.

Step 4. Insert the Terconazole vaginal cream:

  • Lie on your back with knees drawn up toward your chest.
  • Holding the applicator by the ribbed end of the barrel, insert the filled applicator into the vagina as far as it will comfortably go. (See Figure 4)
  • Slowly press the plunger of the applicator to release the cream into the vagina.
  • Remove the applicator from the vagina. Wash the applicator.

Step 5. Wash the Applicator after Use

  • Wash the applicator after each use.
  • Pull the plunger out of the barrel. (See Figure 5)
  • Wash the applicator pieces with lukewarm, soapy water and then dry them very well.
  • Put the dry applicator pieces back together by gently pushing the plunger into the barrel as far as it will go.
Step 6. Wash your hands well after you finish washing and drying the applicator.
Step 7. Repeat Steps 1 through Step 6 until you finish your course of treatment.
Step 8. When you have finished your treatment, throw away (dispose of) the used applicator and tube in your household trash.

Manufactured by:

E. FOUGERA & CO.

A division of Fougera Pharmaceuticals Inc.

Melville, New York 11747

The brands listed are the registered trademarks of their respective owners and are not trademarks of Fougera Pharmaceuticals Inc.

This Instructions for Use has been approved by the U.S Food and Drug Administration Revised: 09/2025

About this document

Source: FDA drug labeling via NLM DailyMed · Application number: NDA 021735 · View the label on DailyMed

Revision date stated in the text: September 2025

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The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Terconazole

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Drug class Azole Antifungal
Active ingredient Terconazole 8 mg/g
Dosage form Cream
Route Vaginal
Marketing status listed in the FDA NDC Directory
Company (applicant) FOUGERA
FDA approval NDA 021735New Drug Application (NDA) Approved October 1, 2004
Reference listed drug This is the reference listed drug (RLD) that generics are compared with.
Therapeutic equivalence (TE) code BXCodes starting with A mean the FDA rates the drug therapeutically equivalent to its reference drug (Orange Book).
Manufacturers 4 labelers list this drug on DailyMed
Packages (NDC)
Package
8 mg/g – 20 g in 1 tube, with applicator NDC 0168-0347-20

Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.