FDA.reportPublic FDA data

FDA label b76aa734-54d8-4a3f-aefd-963d68b1051c

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
d6c85b92-08bc-45de-9cec-43e49c707670
SPL ID
b76aa734-54d8-4a3f-aefd-963d68b1051c
Version
1
Effective date
2011-01-18
Source export date
2026-09-28
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/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:14

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 Avoid contact with eyes Do not apply to wounds or damaged skin Do not bandage tightly Do not use other than as directed Keep out of reach of children to avoid accidental poisoning If swallowed, seek medical help or contact a Poison Control Center right away If condition worsens, or symptoms persist for more than 7 days or clear up and occur again within few days, discontinue use of this product and consult a physician. Do not use if tube seal is broken or appears tampered with.

Reported adverse events (FAERS/openFDA)#

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