FDA label 29233cbb-3fe5-3820-e063-6294a90a5e96

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
71a9a627-7641-486d-884d-a2bd4998d293
SPL ID
29233cbb-3fe5-3820-e063-6294a90a5e96
Version
6
Effective date
2024-12-13
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:15:45

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. ​ If you had prior allergic reaction to aspirin or salicylate, please consult a physician before use. ​Allergy Alert: Do not use • on wounds or damaged skin • with a heating pad. ​you have redness over the affected area. ​Ask a Physician before use if When using this product • avoid contact with eyes and mucus membranes • do not bandage tightly. Stop use and ask a physician if • condition worsens or symptoms persist for more than 7 days • symptoms clear up and occur again within a few days • excessive skin irritation occur • pregnant or breastfeeding. Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Centre right away.

Reported adverse events (FAERS/openFDA)#

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