Home FDA labels 10437086-0291-3a3b-e063-6294a90af4e4 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 ACONITUM NAP., BARYTA CARB., BARYTA MUR., CAPSICUM, CAUSTICUM, CHENOPODIUM ANTHELMINTICUM, CHININUM SULPHURICUM, CINCHONA, GLONOINUM, GRAPHITES, HYDRASTIS, KALI BIC., KALI MUR., LYCOPODIUM, PHOSPHORUS, PULSATILLA, SALICYLICUM AC., TABACUM, THIOSINAMINUM, VIOLA ODORATA
Manufacturer Newton Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 1043debe-8787-a2f5-e063-6294a90a2a66
SPL ID 10437086-0291-3a3b-e063-6294a90af4e4
Version 1
Effective date 2024-01-31
Source export date 2026-10-30
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-30/e37bebe0ee356110e46fe9b102632217cd5fd64caa93a64cf6ef0d92a0bfdb4c/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run 20261102T182004Z
Imported at 2026-11-02 18:51:43 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 · 28 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Ear Ringing openfda.brand_name generic name ACONITUM NAP., BARYTA CARB., BARYTA MUR., CAPSICUM, CAUSTICUM, CHENOPODIUM ANTHELMINTICUM, CHININUM SULPHURICUM, CINCHONA, GLONOINUM, GRAPHITES, HYDRASTIS, KALI BIC., KALI MUR., LYCOPODIUM, PHOSPHORUS, PULSATILLA, SALICYLICUM AC., TABACUM, THIOSINAMINUM, VIOLA ODORATA openfda.generic_name manufacturer name Newton Laboratories, Inc. openfda.manufacturer_name ndc package 55714-2588-1 openfda.package_ndc ndc product 55714-2588 openfda.product_ndc ndc11 package 55714258801 derived:openfda.package_ndc spl id 10437086-0291-3a3b-e063-6294a90af4e4 id spl set id 1043debe-8787-a2f5-e063-6294a90a2a66 set_id unii 27YLU75U4W openfda.unii unii 00UK7646FG openfda.unii unii DD5FO1WKFU openfda.unii unii 4QQN74LH4O openfda.unii unii EL5GJ3U77E openfda.unii unii O414PZ4LPZ openfda.unii unii 6P669D8HQ8 openfda.unii unii 6YR2608RSU openfda.unii unii 4H5RSU087I openfda.unii unii 660YQ98I10 openfda.unii unii ZW3Z11D0JV openfda.unii unii S003A158SB openfda.unii unii U0NQ8555JD openfda.unii unii T4423S18FM openfda.unii unii G59M7S0WS3 openfda.unii unii AET12U8B74 openfda.unii unii 706IDJ14B7 openfda.unii unii I76KB35JEV openfda.unii unii C88X29Y479 openfda.unii unii KF7Z0E0Q2B 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 SECTION WARNINGS : Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feedin g, ask a doctor before use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.