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
2026-09-28
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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:23:08

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.