FDA label 0742f20d-a498-e96f-e063-6394a90a03a3

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
3d924631-af59-42b0-e054-00144ff8d46c
SPL ID
0742f20d-a498-e96f-e063-6394a90a03a3
Version
5
Effective date
2023-10-09
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 06:14:12

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. Use only as directed. • Avoid contact with eyes and mucous membranes. • Do not apply to open wounds or damaged skin. Do not use • in combination with any other external analgesic products.. • Do not use with any bandage, wrap, stocking or similar device or garment. • If symptoms persist for more than 7 days, discontinue use and consult a physician. Keep out of reach of children. • Children under 12 should consult physician prior to use. • If swallowed, consult a physician • Do not bandage tightly. Stop use and consult physician • if symptoms worsen or persist for more than 7 days. If pregnant or breast feeding, • contact physician prior to use.

Reported adverse events (FAERS/openFDA)#

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