FDA label 182f1944-b35a-4d8e-ae28-605f0ba84bec

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
93aa5daf-23b0-4f42-a8c2-f52ba46555f4
SPL ID
182f1944-b35a-4d8e-ae28-605f0ba84bec
Version
32922
Effective date
2024-12-13
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:17:04

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: Discontinue use if any burning, itching, or irritation of the vagina occurs during use. Wash and douche with water. Do not douche to prevent pregnancy. During pregnancy. Do not use during breast feeding. Do not use during period and 4 days after period ends. Children under 12 years of age do not use the product. If swallowed, get medical help or contact a poison control center right away. FOR EXTERNAL USE ONLY. Do not use in eyes.

Reported adverse events (FAERS/openFDA)#

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