FDA label 3062ed70-db5e-427b-81e4-6379beedf4a4

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
e25838f0-c7e2-4504-ab53-58097cf6605a
SPL ID
3062ed70-db5e-427b-81e4-6379beedf4a4
Version
3
Effective date
2023-03-08
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 01:44:17

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. Do not use on wounds or damaged skin or with a heat source. If pregnant or breastfeeding, consult a healthcare professional before use .When using this product: avoid bandaging tightly, avoid contact with eyes, keep out of reach of children. Stop use and ask doctor if: condition worsens, symptoms persist for more than 7 days, symptoms clear up and occur again within a few days.

Reported adverse events (FAERS/openFDA)#

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