FDA label 09543843-1203-4be3-bcf4-675d1dfc4c16

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
2258638a-03ec-46e4-8c9d-fc5d8763150f
SPL ID
09543843-1203-4be3-bcf4-675d1dfc4c16
Version
3
Effective date
2014-11-23
Source export date
2026-10-12
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/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:42:16

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

For external use only. The product should NOT be used on: 1) people who are allergic to the listed ingredients, 2) eye or lip area, 3) infected and flared areas or areas with sensitivity. Store it in a cool, dry place (below 122°F/50°C), away from direct sunlight. Consumers with known bee allergies should NOT use this product as bee venom may induce allergic response(s).

Reported adverse events (FAERS/openFDA)#

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