FDA label 227b98c4-4a7f-4c25-afa3-dc701883ebc4

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
c3067dbd-0fc4-4405-ba1d-fe09010bf89e
SPL ID
227b98c4-4a7f-4c25-afa3-dc701883ebc4
Version
3
Effective date
2021-01-25
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:14:17

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 days. When using this product avoid contact with the eyes. Stop use and ask a doctor if excessive earwax remains after use of this product. 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.