FDA.reportPublic FDA data

FDA label d6a9711e-b627-f1bc-e053-2995a90a8c0f

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
46688e9b-5473-4bda-bcf8-dad206a39d0d
SPL ID
d6a9711e-b627-f1bc-e053-2995a90a8c0f
Version
2
Effective date
2022-01-28
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:41:07

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 2 · 5 matching rows.

warnings

Warnings For External Use Only In case of overdose, get medical help or contact a Poison Control Center right away. Ask a doctor or pharmacist before use if you have any questions about 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 or clear up and occur again within a few days If pregnant or breastfeeding ask a health professional before use.

warnings

Ask a doctor or pharmacist before use if you have any questions about this product

warnings

When using this product Do not get into eyes

warnings

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

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.