FDA label d04d9433-9f2e-336b-e053-2a95a90a8b72

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
c570fbc0-1d0a-4c44-a937-ed8e675f2898
SPL ID
d04d9433-9f2e-336b-e053-2a95a90a8b72
Version
6
Effective date
2021-11-08
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:31:13

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 and cautions

Contraindications/Warnings: Avoid frequent use. Avoid frequent use. Avoid contact with eyes or mucous membranes. Do not apply to open wounds. Should signs of irritation develop, medications should be discontinued. Irritates eyes. nose and throat. Keep out of reach of children. For external use only. Harmful if swallowed. Contact your local poison control center immediately. Do not induce vomiting. If conscious, give eight ounce of (240ml) of milk, or water with activated charcoal.

Reported adverse events (FAERS/openFDA)#

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