Home FDA labels 48bdd1d2-5278-4cb6-aafb-2e54652f6ec4 Cold plus Flu 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 Cold plus Flu
Generic name ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, ANTIMONIUM TARTARICUM, APIS MELLIFICA, BAPTISIA TINCTORIA, BRYONIA (ALBA), EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, LUNG SUIS, SAMBUCUS NIGRA, SERUM ANGUILLAE, STICTA PULMONARIA
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 46193f5d-e9d7-4b34-b69e-d2a490788da0
SPL ID 48bdd1d2-5278-4cb6-aafb-2e54652f6ec4
Version 5
Effective date 2024-07-01
Source export date 2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:55:55 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 · 19 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Cold plus Flu openfda.brand_name generic name ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, ANTIMONIUM TARTARICUM, APIS MELLIFICA, BAPTISIA TINCTORIA, BRYONIA (ALBA), EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, LUNG SUIS, SAMBUCUS NIGRA, SERUM ANGUILLAE, STICTA PULMONARIA openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0247-1 openfda.package_ndc ndc product 50845-0247 openfda.product_ndc ndc11 package 50845024701 derived:openfda.package_ndc spl id 48bdd1d2-5278-4cb6-aafb-2e54652f6ec4 id spl set id 46193f5d-e9d7-4b34-b69e-d2a490788da0 set_id unii 7GL3G1COB3 openfda.unii unii 639KR60Q1Q openfda.unii unii DL6OZ476V3 openfda.unii unii L7B16ESD1U openfda.unii unii T7J046YI2B openfda.unii unii RN2HC612GY openfda.unii unii CT03BSA18U openfda.unii unii 1W0775VX6E openfda.unii unii 5EF0HWI5WU openfda.unii unii 7S82P3R43Z openfda.unii unii D1YM0P5Z2T 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 3 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 health professional before use. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.