FDA label 6d395f97-13b3-4f1b-86c2-f7dff46cdeb9

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
d7a5e7db-6299-4577-b179-cdc05ee17ce6
SPL ID
6d395f97-13b3-4f1b-86c2-f7dff46cdeb9
Version
3
Effective date
2020-05-29
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 01:43:01

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, ask a doctor before use When using this product use only as directed avoid getting into the eyes and mucous membranes do not bandage tightly or use with a heating pad do not apply to wounds or damaged skin Stop use and ask doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days excessive skin irritation or redness occurs If pregnant of breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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