FDA label ebd958f3-8205-430e-9f2b-a67e5ffa4995

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
33d4150c-9fe5-40b5-b0d5-210e0c6eba2b
SPL ID
ebd958f3-8205-430e-9f2b-a67e5ffa4995
Version
2
Effective date
2012-08-03
Source export date
2026-11-06
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:30:23

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 Warning For External Use Only Do not use In the eye for more than 4 days Ask a doctor before use if you have ear drainage or discharge pain, irritation or rash in the ear had ear surgery an injury or perforation (hole) in the ear drum Stop use and ask a doctor if Stop use and ask a doctor if excessive earwax remains after use 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.