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
2026-11-06
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/2026-11-06/bbdc0a42bf44145a63c3752991067bece7e2a518be6cc14943d33c4987faa012/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:11:07

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.