FDA label 155d4a58-de2f-4948-9904-c91d19768b96

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
b8391091-e454-45f6-b5e3-8ded40855a90
SPL ID
155d4a58-de2f-4948-9904-c91d19768b96
Version
2
Effective date
2018-03-06
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:35:06

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 the eyes • over large areas of the body When using this product • keep out of eyes. Rinse with water to remove. • do not puncture or incinerate. Contents under pressure. ​Ask a doctor before use if you have • deep or puncture wounds • animal bites • serious burns ​Stop use and ask a doctor if ​ ​ • condition or simptoms get worse or last more than one week • symptoms clear up and occur again within a few days Keep out of reach of the children . If product is 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.