FDA label a1245ff9-2a14-177a-e053-2995a90a5a9f

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
63b20a8c-c520-1949-e053-2a91aa0a4ca4
SPL ID
a1245ff9-2a14-177a-e053-2995a90a5a9f
Version
2
Effective date
2020-03-18
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 05:16:12

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

For external use only. Do not use with other topical pain relivers with heating pads or heating devices When using this product do not use in or near the eyes do not apply to wounds or damaged skin do not bandage tightly Stop use and ask a doctor if: condition worsens symptoms last more than 7 days or clear up and occur again within a few days redness or iritation develops It 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.