FDA label dfe6f1ef-78fa-4ded-8d8b-47c4bfa19300

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
e5146399-6c16-44e4-8c95-79c1d32a42e9
SPL ID
dfe6f1ef-78fa-4ded-8d8b-47c4bfa19300
Version
5
Effective date
2017-12-04
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:59:46

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 Allergy alert: do not use if allergic to any of the ingredients Do not use in the eyes over large areas of the body Ask a doctor before use if you have deep or puncture wounds animal bites serious burns When using this product do not use longer than 1 week unless directed by a doctor Stop use and ask a doctor if condition persists or gets worse symptoms last for more than 7 days or clear up and occur again within a few days a rash or other allergic reaction occurs 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.