FDA label 918a70cd-b444-42e7-81c2-fb1db759f278

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
b367d572-89f3-44e5-99a5-ddba71e28fc0
SPL ID
918a70cd-b444-42e7-81c2-fb1db759f278
Version
3
Effective date
2014-06-06
Source export date
2026-10-12
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/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:33:56

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

Consumers with known bee allergies should NOT use this product as bee venom may cause an allergic reaction. Do not apply to wounded or infected areas. If irritation develops, discontinue use and consult a physician immediately. Keep out of reach of children. Close lid after each use. Store in a cool, dry place away from direct sunlight.

Reported adverse events (FAERS/openFDA)#

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