FDA label 38f08449-a930-4b45-bd55-8463a5696d9b

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
3f2767e9-8223-6c15-e054-00144ff8d46c
SPL ID
38f08449-a930-4b45-bd55-8463a5696d9b
Version
4
Effective date
2018-11-08
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:42:00

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 in eyes or apply over large areas of the body. In case of deep or punture wounds, amimal bites or serious burns, consult a physician. Do not ingest. STOP USE AND ASK A DENSTIST OR A PHYSICIAN if condition persits or worsens or if symptoms persist for more than 7 days. WHEN USING THIS PRODOCT you may feel a tingling or stinging sensation which should go away in a short time. keep out of reach of children and in case of allergic reaction, get medical help or contact a poison control center immediately. 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.