FDA label cc3890bf-7ef6-4c8e-9bec-66b0eb1a9916

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
389e27c8-f16a-4028-92b4-813a26114d15
SPL ID
cc3890bf-7ef6-4c8e-9bec-66b0eb1a9916
Version
3
Effective date
2025-06-14
Source export date
2026-10-12
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:56:58

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: On deep or puncture wounds On animal bites On serious burns Ask a doctor before use if you have: A serious wound or condition that requires medical attention When using this product Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if Condition worsens Symptoms last more than 7 days or clear up and occur again within a few days You are allergic to any of the ingredients in this product 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.