FDA.reportPublic FDA data

FDA label 06caa424-56ef-4b31-a226-14db9ee4a457

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
d7eb7100-d83b-4b4b-8868-ecb630d8e7b1
SPL ID
06caa424-56ef-4b31-a226-14db9ee4a457
Version
9
Effective date
2011-12-28
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 02:49:03

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 Ask a doctor before use if Ask a doctor or pharmacist before use if When using this product Avoid contact with eyes; in case of contact, thoroughly rinse eyes with water. Seek medical attention if irritation persists. Stop use and ask a doctor if skin rash or redness develops when using this product Pregnancy/Breastfeeding 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.