FDA.reportPublic FDA data

FDA label 66989f80-e8b6-4af5-997c-5546ea4cc3d6

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
2cccc07a-80f3-4de4-b31a-87aba0c11e42
SPL ID
66989f80-e8b6-4af5-997c-5546ea4cc3d6
Version
2
Effective date
2016-09-15
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:12:49

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 • with other topical pain relievers • with heating pads or heating devices. When using this product • do not use in or near 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 irritation develops 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.