FDA label d93b9e18-b3a1-4b72-b1fa-48932a2d9b49

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
627edb87-63a1-4be2-860d-07514e27d7ad
SPL ID
d93b9e18-b3a1-4b72-b1fa-48932a2d9b49
Version
1
Effective date
2021-03-10
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:04:17

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 Flammable: Keep away from fire or flame For external use only. Do not use • on wounds or damaged skin. When using this product • avoid contact with the eyes. If contact occurs, rinse with water to remove • do not bandage tightly Stop use and ask a doctor if • condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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