Home FDA labels f7a1859f-8cf8-4dd7-9497-ddc26a9f5388 Cough plus Bronchial 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 Cough plus Bronchial
Generic name ANTIMONIUM TARTARICUM, ARUM TRIPHYLLUM, BADIAGA, BAPTISIA TINCTORIA, BRYONIA (ALBA), DROSERA (ROTUNDIFOLIA), ECHINACEA (ANGUSTIFOLIA), EUPATORIUM PERFOLIATUM, KALI BROMATUM, LUNG SUIS, PHOSPHORUS, PULSATILLA (PRATENSIS), SPONGIA TOSTA, STICTA PULMONARIA, SULPHUR IODATUM, URTICA URENS
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 801eba42-4217-46e9-8f3e-745da01a27b0
SPL ID f7a1859f-8cf8-4dd7-9497-ddc26a9f5388
Version 6
Effective date 2024-07-01
Source export date 2026-10-12
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/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:28:14 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Cough plus Bronchial openfda.brand_name generic name ANTIMONIUM TARTARICUM, ARUM TRIPHYLLUM, BADIAGA, BAPTISIA TINCTORIA, BRYONIA (ALBA), DROSERA (ROTUNDIFOLIA), ECHINACEA (ANGUSTIFOLIA), EUPATORIUM PERFOLIATUM, KALI BROMATUM, LUNG SUIS, PHOSPHORUS, PULSATILLA (PRATENSIS), SPONGIA TOSTA, STICTA PULMONARIA, SULPHUR IODATUM, URTICA URENS openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0246-1 openfda.package_ndc ndc product 50845-0246 openfda.product_ndc ndc11 package 50845024601 derived:openfda.package_ndc spl id f7a1859f-8cf8-4dd7-9497-ddc26a9f5388 id spl set id 801eba42-4217-46e9-8f3e-745da01a27b0 set_id unii 27YLU75U4W openfda.unii unii 7GL3G1COB3 openfda.unii unii 6SZ0G98BHM openfda.unii unii OSD78555ZM openfda.unii unii QR44N9XPJQ openfda.unii unii DL6OZ476V3 openfda.unii unii ETJ7Z6XBU4 openfda.unii unii IHN2NQ5OF9 openfda.unii unii VB06AV5US8 openfda.unii unii 8E272251DI openfda.unii unii T7J046YI2B openfda.unii unii 1W0775VX6E openfda.unii unii 1PIP394IID openfda.unii unii 5EF0HWI5WU openfda.unii unii L6L8KA2AA0 openfda.unii unii D1YM0P5Z2T openfda.unii unii DM64K844DM 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: Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Stop use and ask a doctor if cough persists for more than one (1) week, tends to recur, or if it is accompanied by fever, rash or by persistent headache. A persistent cough may be a sign of a serious condition. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. If pregnant or breast feeding, ask a doctor before using product. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken. Other information Store at room temperature.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.