FDA label 55759e87-5b00-4479-99d4-2feee369e586

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
81892ea2-9863-4db2-844a-6587b5bbfd9d
SPL ID
55759e87-5b00-4479-99d4-2feee369e586
Version
3
Effective date
2018-03-27
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 01:42:28

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. Do not use • on wounds or damaged skin • with a heating pad • if you are allergic to any ingredients of this product When using this product • use only as directed • avoid contact with eyes, mucous membranes or rashes • do not bandage tightly Stop use and ask a doctor if • rash, itching or excessive skin irritation develops • conditions worsen • 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.