FDA label e67e0338-9608-4f5e-a4d2-6e8676e07e7a

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
20afe385-0ddb-40d3-a9bb-29bbc373b8a8
SPL ID
e67e0338-9608-4f5e-a4d2-6e8676e07e7a
Version
2
Effective date
2014-10-15
Source export date
2026-10-12
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:49:42

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.