FDA label d5483a8e-e04b-b371-e053-2a95a90aaf6a

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
bf3eff1d-53ef-2ea0-e053-2995a90a5dca
SPL ID
d5483a8e-e04b-b371-e053-2a95a90aaf6a
Version
5
Effective date
2022-01-10
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:43:26

Warnings cross-check#

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

Warnings sections page 1 of 1 · 2 matching rows.

warnings

WARNING For external use on the skin only. Severe injury may result from use internally or as a douche. Avoid contact with mucous membranes."

warnings and cautions

WARNINGS AND PRECAUTIONS There may be moderate burning or pain after the first applications of the solution, which usually disappear with the continuation of the treatment.

Reported adverse events (FAERS/openFDA)#

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