FDA label 6791d4f2-c485-4daf-82c7-0cafa9a7a17d

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
6791d4f2-c485-4daf-82c7-0cafa9a7a17d
SPL ID
6791d4f2-c485-4daf-82c7-0cafa9a7a17d
Version
1
Effective date
2011-02-17
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:48:18

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For vaginal use only Ask a doctor before use if you have . never had a vaginal yeast infection diagnosed by a doctor . 1 or more of the following: abdominal pain, fever, chills, nausea, vomiting, foul-smelling vaginal discharge . vaginal yeast infections often (such as once a month or 3 in 6 months) . been exposed to the human immunodeficiency virus (HIV) that causes AIDS Ask a doctor or pharmacist before use if you are taking the prescription blood thinning medication warfarin, because bleeding or bruising may occur. When using this product . do not use tampons, douches, spermicides, or other vaginal products . do not have vaginal intercourse . condoms and diaphragms may be damaged and fail to prevent pregnancy or sexually transmitted diseases (STDs) Stop use and ask a doctor if . symptoms do not get better in 3 days . symptoms last more than 7 days . you get abdominal pain, fever, chills, nausea, vomiting, foul-smelling vaginal discharge, or rash If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.