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
2026-11-06
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/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:57:14

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.