FDA label d122b9b5-cde6-21d2-e053-2995a90a76da

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
d122b9b5-cde5-21d2-e053-2995a90a76da
SPL ID
d122b9b5-cde6-21d2-e053-2995a90a76da
Version
1
Effective date
2021-11-22
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 05:23:30

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 1.Those who are allergic to this product and minors are forbidden. 2.This product is a topical productand it is forbidden to take it orally. 3.Should not be used for the prevention of sexually transmitted diseases in sexual life. 4.Do not use on damaged mucosa wounds. 5.This productis a topical product and cannot be used as a substitute for drugs. 6.A small amount of precipitation during storage is normal and does not affect use.

Reported adverse events (FAERS/openFDA)#

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