FDA.reportPublic FDA data

FDA label 575bf24b-6075-7490-e053-2991aa0a1993

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
575bf24b-6074-7490-e053-2991aa0a1993
SPL ID
575bf24b-6075-7490-e053-2991aa0a1993
Version
1
Effective date
2017-08-22
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:02:00

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 Do not use if you have/are pregnat, hypersensitivity to any pain. When using this product - do not use during menstruation - use clean underwear - do not use tampons, douches, condoms, feminine clenasers, or other vaginal products - do not eat or swallow Stop use and ask a doctor if - symptoms get worsen or do not get better - symptoms last more than 7days - you get rashes or hives, abdominal pain, fever, chillis, nausea, vomiting or foul-smelling vaginal odor or discharge Store at room tmperature and in a dry place.

Reported adverse events (FAERS/openFDA)#

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