FDA label 29959122-4c28-278e-e063-6394a90a4cd3

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
557c72cb-0f93-4c84-aec2-cc42735b232f
SPL ID
29959122-4c28-278e-e063-6394a90a4cd3
Version
9
Effective date
2023-12-02
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:10:49

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 external use only. When using this product: • Do not get into eyes. • Test on a small area of your forearm before use. • Propolis may cause skin irritation. • Discontinue use if rash appears. • This product should not be used in or around the eyes. • Do not use if allergic to bee stings or bee by-products. Stop use and ask a doctor if: • Condition worsens. • Symptoms last more than 7 days or clear up and occur again within a few days. • As with any product, ask a doctor before use if pregnant or breast-feeding. Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

Reported adverse events (FAERS/openFDA)#

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