FDA label 84b64407-c9d7-4c60-e053-2991aa0afaac

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
64c97569-0485-4136-8fe7-8be4babd8973
SPL ID
84b64407-c9d7-4c60-e053-2991aa0afaac
Version
3
Effective date
2019-03-22
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:52:39

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: Do not use if you are allergic to salicylates (including aspirin) unless directed by a doctor. When using this product Use only as directed Do not bandage tightly or use a heating pad Avoid contact with eyes or mucous membranes Do not apply to wounds or damaged skin Stop use and ask a doctor if Condition worsens Symptoms persist for more than 7 days or clear up and occur again within a few days Redness is present Irritation develops If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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