FDA label 6001c9f5-8e34-2c06-e053-2a91aa0a6542

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
3c4f2997-20d6-4970-a6ba-a59a5e227127
SPL ID
6001c9f5-8e34-2c06-e053-2a91aa0a6542
Version
16
Effective date
2017-12-10
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:07:57

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

For external use only Do not use in the eyes or apply over large areas of the body longer than 1 week unless directed by a doctor in large quantities, particularly over raw surfaces or blistered areas Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns When using this product avoid contact with eyes Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days condition clears up and occurs again within a few days 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.