FDA.reportPublic FDA data

FDA label 796d462e-1176-46b1-93a7-086b4c8abde9

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
b3f6fc16-4d5e-4178-863e-c3b3db95a99d
SPL ID
796d462e-1176-46b1-93a7-086b4c8abde9
Version
3
Effective date
2025-07-19
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:45:25

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 children under 2 years of age unless directed by a doctor near eyes or mucous membranes When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water. if irritation or rash develops, stop use and consult a doctor. Stop use and ask a doctor if If irritation or rash develops, stop use and consult a doctor. 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.