FDA label bbb53552-fd40-a688-e053-2995a90a2a66

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
42190b8a-2c1a-4cdf-8752-120b5dee3b94
SPL ID
bbb53552-fd40-a688-e053-2995a90a2a66
Version
1
Effective date
2021-02-19
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:16:10

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

Warning For external use only. Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use. Stop use and ask a doctor if condition worsens or if symptoms persist for more than 7 days or clear up and occurs again within a few days. Redness is present. Excessive irritation of the skin develops. When using this product Use only as directed. Avoid contact with the eyes or mucous membranes. Do not apply on wounds and damaged skin. Do not bandage tightly. Do not use with heating pad. If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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