FDA label 689f5f69-93be-40fe-e053-2991aa0a0bf0

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
dc5a4c2f-6dcd-4e04-b551-f0703ef6c7e3
SPL ID
689f5f69-93be-40fe-e053-2991aa0a0bf0
Version
3
Effective date
2018-03-30
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 06:11:37

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. Avoid contact with eyes. Do not apply to wounds or damaged skin. Do not use with bandage, wrap, brace, stocking or similar device or garment. Do not use in combination with any other external analgesic products. If symptoms persist for more than seven days, discontinue use and consult a physician. Keep out of reach of children . If swallowed, consult physician. Do not bandage tightly. If pregnant of breast feeding, contact physician prior to use.

Reported adverse events (FAERS/openFDA)#

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