Home FDA labels 2fb50204-f6e9-4d7a-a79e-21aaa81f8096 Ear Ring 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 Ring
Generic name ALLIUM CEPA, ARGENTUM NITRICUM, ASARUM CANADENSE, CARBO VEGETABILIS, CARBONEUM SULPHURATUM, CARTILAGO SUIS, CHENOPODIUM ANTHELMINTICUM, CHININUM SULPHURICUM, CYCLAMEN EUROPAEUM, DULCAMARA, GINKGO BILOBA, GRAPHITES, KREOSOTUM, MUCOSA NASALIS SUIS, NATRUM SALICYLICUM, PHOSPHORUS, PLUMBUM METALLICUM, THERIDION, ZINCUM METALLICUM
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID c4b66b0a-fb00-4047-af7e-b5b0f2327f2f
SPL ID 2fb50204-f6e9-4d7a-a79e-21aaa81f8096
Version 3
Effective date 2025-04-29
Source export date 2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:14:26 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 · 27 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Ear Ring openfda.brand_name generic name ALLIUM CEPA, ARGENTUM NITRICUM, ASARUM CANADENSE, CARBO VEGETABILIS, CARBONEUM SULPHURATUM, CARTILAGO SUIS, CHENOPODIUM ANTHELMINTICUM, CHININUM SULPHURICUM, CYCLAMEN EUROPAEUM, DULCAMARA, GINKGO BILOBA, GRAPHITES, KREOSOTUM, MUCOSA NASALIS SUIS, NATRUM SALICYLICUM, PHOSPHORUS, PLUMBUM METALLICUM, THERIDION, ZINCUM METALLICUM openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-2264-1 openfda.package_ndc ndc product 43742-2264 openfda.product_ndc ndc11 package 43742226401 derived:openfda.package_ndc spl id 2fb50204-f6e9-4d7a-a79e-21aaa81f8096 id spl set id c4b66b0a-fb00-4047-af7e-b5b0f2327f2f set_id unii 2P3VWU3H10 openfda.unii unii 27YLU75U4W openfda.unii unii E2O4O7TQYK openfda.unii unii KPS1B1162N openfda.unii unii 4QQN74LH4O openfda.unii unii G728143D8Q openfda.unii unii WIQ1H85SYP openfda.unii unii S54S8B99E8 openfda.unii unii ID3Z1X61WY openfda.unii unii 95IT3W8JZE openfda.unii unii 4H5RSU087I openfda.unii unii 73ECW5WG2F openfda.unii unii 492225Q21H openfda.unii unii 2P299V784P openfda.unii unii 19FUJ2C58T openfda.unii unii 3JYG22FD73 openfda.unii unii 9Z8D3HEM8L openfda.unii unii J41CSQ7QDS 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: If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.