FDA label bf074850-bc6d-56c1-e053-2995a90ad12f

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
01833c1d-6bf9-4c25-8f6c-3ba132f1e4c6
SPL ID
bf074850-bc6d-56c1-e053-2995a90ad12f
Version
1
Effective date
2021-04-02
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:16:09

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 if allergic to any ingredients of this product When using this product do not get into eyes Stop use and ask a doctor if condition worsens symptoms last more than 7 days symptoms clear up and occur again within a few days excessive irritation of the skin develops side effects occur. You may report side effects to FDA at 1–800–FDA–1088. Keep out of reach of children to avoid accidental poisoning . 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.