FDA.reportPublic FDA data

FDA label 37de3de4-40bd-bb6f-e063-6394a90a282c

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
3685378e-b0c8-6ce1-e063-6394a90ad2b7
SPL ID
37de3de4-40bd-bb6f-e063-6394a90a282c
Version
2
Effective date
2025-06-18
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:25:08

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: Warnings For vaginal use only. Not for oral consumption. Do not use If you are allergic to any of the ingredients. When using this product do not exceed the recommended dose. Ask a doctor before use If you have irregular menstrual cycles not related to menopause • If you are taking hormone replacement therapy (HRT) or other medications Stop use and ask a doctor If symptoms persist for more than 7 days or worsen If new symptoms occur If you experience an allergic reaction

Reported adverse events (FAERS/openFDA)#

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