FDA label 843ead7f-6cf7-47da-8d8b-eba5d035bc37

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
5c5023bd-b445-4025-9a5b-774e6a7e67a4
SPL ID
843ead7f-6cf7-47da-8d8b-eba5d035bc37
Version
1
Effective date
2014-02-27
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:35:27

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 ■ On infected or damaged skin When using this product: ■ Avoid contact with eyes or mucous membranes. ■ Do not bandage tightly. Stop use and ask a doctor if: ■ Condition worsens ■ Symptom clear up and occur again within a few days. ■ Symptom persist for more than 7 days. ■ Nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs ■ Excessive irritation of the skin develops ■ When using for pain of arthritis: ■ In conditions affecting children under 12 years of age ■ If redness is present ■ If pain persists for more than 10 days

Reported adverse events (FAERS/openFDA)#

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