FDA label 003de20a-3ba2-442a-a56f-c79b9f723b9e

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
981d8665-c8d0-4dbc-9d3c-c36be81ad102
SPL ID
003de20a-3ba2-442a-a56f-c79b9f723b9e
Version
8
Effective date
2011-02-04
Source export date
2026-10-12
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/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:30:18

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

From Warnings Section of Carton Label: Warnings For external use only. ______________________________ Ask a doctor before use on children under 2 years of age ____________________________________ When using this product avoid contact with the eyes ____________________________________ Stop use and consult a doctor if - Irritation occurs - you do not notice improvement within 4 weeks ____________________________________ KEEP THIS AND ALL MEDICATION OUT OF THE REACH OF CHILDREN If accidental ingestion occurs, immediately contact a physician, emergency medical facility or Poison Control Center for help.

Reported adverse events (FAERS/openFDA)#

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