FDA label e48d9a80-92a3-489e-9eef-222b9dc6d0ef

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
53a1e60f-f641-4aed-874a-efcb13dc1074
SPL ID
e48d9a80-92a3-489e-9eef-222b9dc6d0ef
Version
2
Effective date
2023-06-07
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 05:58:12

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. Do Not Use: On wounds or damaged skin, with a heating pad, or on a child under 12 years of age with arthritis-like conditions. Ask a Doctor Before Use If You Have: Redness over the affected area. When Using This Product: Avoid contact with eyes or mucous membranes; do not bandage tightly. Stop Use and Ask Doctor If: Condition worsens or symptoms persist for more than 7 days, if symptoms clear up and occur again within a few days, or if redness is present or excessive skin irritation develops. CAUTION: Keep away from eyes. Wash hands and fingers thoroughly.

Reported adverse events (FAERS/openFDA)#

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