FDA.reportPublic FDA data

FDA label 8954ed77-7d80-1f0a-e053-2a95a90a4d71

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
8241a644-9e60-22fb-e053-2991aa0a1bfa
SPL ID
8954ed77-7d80-1f0a-e053-2a95a90a4d71
Version
2
Effective date
2019-05-20
Source export date
2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:51:00

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 Warnings Do Not Use and consult a doctor if you have excessive drainage or discharge ear pain, irritation, or rash in the ear or feel dizzy. Do not use if you have an perforation (hole) of the eardrum or after ear surger unless directed by a doctor. Do not use for more than four days. If excessive earwax remains after use of this products, consult a doctor. Image Reference: Clear Canal Earwax Softner Drop Product Label.jpg Clear Canal Earwax Softner Drops Outer box carton.jpg

Reported adverse events (FAERS/openFDA)#

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