Home FDA labels 4cbd2be4-23e5-4103-af78-8aa5c2ae34a4 Ear Ringing 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)
Brand name Ear Ringing
Generic name ARNICA MONTANA, CALCAREA CARBONICA, CHENOPODIUM ANTH, CHININUM SALICYLICUM, CIMICIFUGA RACEMOSA, COFFEA TOSTA, KALI IODATUM, KALMIA LATIFOLIA, MAGNESIA CARBONICA, MANGANUM ACETICUM, MANGANUM CARBONICUM, MERCURIUS VIVUS, NATRUM SALICYLICUM, SALICYLICUM ACIDUM, THIOSINAMINUM, AND THYROIDINUM.
Manufacturer King Bio Inc.
Product type HUMAN OTC DRUG
SPL set ID 4227b9a3-b0c1-4c74-9edd-922e32e6e89d
SPL ID 4cbd2be4-23e5-4103-af78-8aa5c2ae34a4
Version 1
Effective date 2026-03-04
Source export date 2026-09-28
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:15:40 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Ear Ringing openfda.brand_name generic name ARNICA MONTANA, CALCAREA CARBONICA, CHENOPODIUM ANTH, CHININUM SALICYLICUM, CIMICIFUGA RACEMOSA, COFFEA TOSTA, KALI IODATUM, KALMIA LATIFOLIA, MAGNESIA CARBONICA, MANGANUM ACETICUM, MANGANUM CARBONICUM, MERCURIUS VIVUS, NATRUM SALICYLICUM, SALICYLICUM ACIDUM, THIOSINAMINUM, AND THYROIDINUM. openfda.generic_name manufacturer name King Bio Inc. openfda.manufacturer_name ndc package 57955-9978-2 openfda.package_ndc ndc product 57955-9978 openfda.product_ndc ndc11 package 57955997802 derived:openfda.package_ndc spl id 4cbd2be4-23e5-4103-af78-8aa5c2ae34a4 id spl set id 4227b9a3-b0c1-4c74-9edd-922e32e6e89d set_id unii 6DY04L71DR openfda.unii unii 9H58JRT35E openfda.unii unii 0B4FDL9I6P openfda.unii unii O80TY208ZW openfda.unii unii O414PZ4LPZ openfda.unii unii 79N6542N18 openfda.unii unii WIQ1H85SYP openfda.unii unii FXS1BY2PGL openfda.unii unii 0E53J927NA openfda.unii unii 4H5RSU087I openfda.unii unii 9TO51D176N openfda.unii unii 2E32821G6I openfda.unii unii 1C4QK22F9J openfda.unii unii 706IDJ14B7 openfda.unii unii 9ZV57512ZM openfda.unii unii K73E24S6X9 openfda.unii
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 Stop use and consult a doctor if symptoms worsen or persist for more than 7 days. If pregnant or breast-feeding, ask a healthcare professional before use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.