FDA.reportPublic FDA data

FDA label 8d78e20a-bfdc-49ca-bcbf-ba2526b2cd13

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
98300b16-36d2-4d50-8b9d-77740b871a47
SPL ID
8d78e20a-bfdc-49ca-bcbf-ba2526b2cd13
Version
4
Effective date
2018-09-14
Source export date
2026-08-01
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/286b06ef66f7efdb8cdf48688678b429950d1b94558fe44fcd6cc6eb20c2100b/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:05:26

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 For oral use only. Blood in urine, fever, nausea, vomiting, pain in kidney area or acute urinary retention may be serious. Consult a doctor promptly if any of these symptoms occur. Do not use if you are allergic to bee venom Stop use and ask a doctor if symptoms persist for more than 5 days, worsen or new symptoms occur. If pregnant or breast-feeding, ask a health professional before use. Keep this and all medicines out of reach of children. In case of accidental overdose, seek professional assistance or contact a poison control center immediately.