FDA label 232937b5-93d7-4d74-b15e-23fdb2a39590

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
392378b5-c5c1-41e0-aac1-800dfeee8142
SPL ID
232937b5-93d7-4d74-b15e-23fdb2a39590
Version
1
Effective date
2015-07-22
Source export date
2026-10-12
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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:48:45

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 eardrum or after ear surgery, unless directed by a doctor. •for more than four consecutive days. When using this product •avoid contact with the eyes. Stop use and ask a doctor if • excessive ear wax remains after use of this product for four consecutive days. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If accidental contact with eyes occurs, flush eyes with water and consult a doctor.

Reported adverse events (FAERS/openFDA)#

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