FDA label fe25dac9-75fc-eb72-e053-6394a90ace4e

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
de33bc28-4f67-4f83-9da1-fad76b675f07
SPL ID
fe25dac9-75fc-eb72-e053-6394a90ace4e
Version
4
Effective date
2023-06-15
Source export date
2026-08-01
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/928e480b2a9ec5fd356ebc3e5dcca70f0f57b8a051cfbb174a4421de39bb77a2/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:26:33

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 . • Allergy Alert If prone to allergic reaction from aspirin or salicylates, consult a doctor before use. When using this product •use only as directed •do not bandage tightly or use with a heating pad •avoid contact with eyes or mucous membranes • do not apply to wounds or damaged skin. Stop use and ask a doctor if condition worsens •symptoms persist for more than 7 days or clear up and occur again within a few days •redness is persistent •irritation develops.