Home FDA labels 6c71b14c-9ef4-47e9-8042-41d95a20453a Sinus Congestion Headache 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 Sinus Congestion Headache
Generic name ANTIMONIUM TARTARICUM, ASAFOETIDA, BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), EUPATORIUM PERFOLIATUM, EUPHORBIA PILULIFERA, HEPAR SULPHURIS CALCAREUM, HYDRASTIS CANADENSIS, IODIUM, KALI BICHROMICUM, LACHESIS MUTUS, MAGNESIA CARBONICA, MUCOSA NASALIS SUIS, PULSATILLA (PRATENSIS), PYROGENIUM, SILICEA, TEUCRIUM MARUM
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID debc7747-8664-4598-a862-e295188c4fca
SPL ID 6c71b14c-9ef4-47e9-8042-41d95a20453a
Version 3
Effective date 2024-11-04
Source export date 2026-10-12
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:44:55 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 Sinus Congestion Headache openfda.brand_name generic name ANTIMONIUM TARTARICUM, ASAFOETIDA, BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), EUPATORIUM PERFOLIATUM, EUPHORBIA PILULIFERA, HEPAR SULPHURIS CALCAREUM, HYDRASTIS CANADENSIS, IODIUM, KALI BICHROMICUM, LACHESIS MUTUS, MAGNESIA CARBONICA, MUCOSA NASALIS SUIS, PULSATILLA (PRATENSIS), PYROGENIUM, SILICEA, TEUCRIUM MARUM openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0263-1 openfda.package_ndc ndc package 50845-0263-2 openfda.package_ndc ndc product 50845-0263 openfda.product_ndc ndc11 package 50845026302 derived:openfda.package_ndc ndc11 package 50845026301 derived:openfda.package_ndc spl id 6c71b14c-9ef4-47e9-8042-41d95a20453a id spl set id debc7747-8664-4598-a862-e295188c4fca set_id unii DL6OZ476V3 openfda.unii unii 29SUH5R3HU openfda.unii unii ID3Z1X61WY openfda.unii unii 9679TC07X4 openfda.unii unii ETJ7Z6XBU4 openfda.unii unii W9FZA51AS1 openfda.unii unii 0E53J927NA openfda.unii unii 6H89ZY31MR openfda.unii unii VB06AV5US8 openfda.unii unii 8E272251DI openfda.unii unii ZW3Z11D0JV openfda.unii unii VSW71SS07I openfda.unii unii T4423S18FM openfda.unii unii 1W0775VX6E openfda.unii unii 10464S0TAA openfda.unii unii 5EF0HWI5WU openfda.unii unii 1MBW07J51Q 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 symptoms persist for more than 7 days, worsen or if new symptoms occur. 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 this product. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken. Store at room temperature.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.