FDA label 7e00e69c-457a-c339-e053-2991aa0a5efa

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
717e5908-86f2-713e-e053-2995a90a5149
SPL ID
7e00e69c-457a-c339-e053-2991aa0a5efa
Version
2
Effective date
2018-12-31
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:42:12

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, External use only, do not take it orally. 2, Can not be used to prevent the venereal disease. 3, A few sediment is normal phenomenon, do not effect the use. 4, Keep out of reach of children. 5, If irritation or discomfort occurs, discontinue the use and consult a physician. 6, Do not use if quality seal on the opening of the tube is broken or missing. 7, Keep it sealed and place it in shady place.

Reported adverse events (FAERS/openFDA)#

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