FDA label f2c3033a-b17f-4cd6-97c2-d5f4d204da63

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
abfbf016-fda2-44a3-8bd7-be5eb9cd8b99
SPL ID
f2c3033a-b17f-4cd6-97c2-d5f4d204da63
Version
1
Effective date
2018-08-16
Source export date
2026-11-06
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:59:38

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 Do not use • if you have ear drainage or discharge, ear pain, irritation or rash in the ear, or are dizzy; consult a doctor. • if you have an injury or perforation (hole) of the ear drum or after ear surgery unless directed by a doctor. • for more than four consecutive days. When using this product • avoid contact with eyes Stop use and ask a doctor if • excessive ear wax remains after use of this product for four consecutive days

Reported adverse events (FAERS/openFDA)#

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