FDA.reportPublic FDA data

FDA label 3f268739-25d7-09be-e054-00144ff88e88

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
5b599999-5af2-4771-bce9-77810db0c268
SPL ID
3f268739-25d7-09be-e054-00144ff88e88
Version
8
Effective date
2016-10-18
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:02:10

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.