FDA.reportPublic FDA data

FDA label bb3695e0-de0f-4a74-ada1-fe313d5f85ff

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
132b36dc-e896-4407-9001-7f243336d46c
SPL ID
bb3695e0-de0f-4a74-ada1-fe313d5f85ff
Version
2
Effective date
2012-06-18
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:58:46

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 mucuous membranes, and do not apply to wounds or damaged skin. Stop use and ask doctor if : condition gets worse, symptoms persist for more than 7 days, or symptoms clear up and occur again in a few days, redness is present, or irritation develops.

Reported adverse events (FAERS/openFDA)#

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