Home FDA labels b5aaba49-f865-3b55-e053-2995a90abcf4 MacDee 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 MacDee
Generic name ACONITUM NAPELLUS, AURUM METALLICUM, BARYTA CARBONICA, BELLADONNA, CROTALUS HORRIDUS, EUPHRASIA OFFICINALIS, GELSEMIUM SEMPERVIRENS, HAMAMELIS VIRGINIANA, LACHESIS MUTUS, MERCURIUS VIVUS, PHOSPHORUS, PICRICUM ACIDUM, PLUMBUM METALLICUM, PULSATILLA, RHUS TOXICODENDRON, STRAMONIUM, THERIDION, ELAPS CORALLINUS.
Manufacturer Newton Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 9a6409d4-89f3-1ab8-e053-2995a90a3f1f
SPL ID b5aaba49-f865-3b55-e053-2995a90abcf4
Version 2
Effective date 2020-12-04
Source export date 2026-10-12
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:32:34 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 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name MacDee openfda.brand_name generic name ACONITUM NAPELLUS, AURUM METALLICUM, BARYTA CARBONICA, BELLADONNA, CROTALUS HORRIDUS, EUPHRASIA OFFICINALIS, GELSEMIUM SEMPERVIRENS, HAMAMELIS VIRGINIANA, LACHESIS MUTUS, MERCURIUS VIVUS, PHOSPHORUS, PICRICUM ACIDUM, PLUMBUM METALLICUM, PULSATILLA, RHUS TOXICODENDRON, STRAMONIUM, THERIDION, ELAPS CORALLINUS. openfda.generic_name manufacturer name Newton Laboratories, Inc. openfda.manufacturer_name ndc package 55714-4827-1 openfda.package_ndc ndc product 55714-4827 openfda.product_ndc ndc11 package 55714482701 derived:openfda.package_ndc spl id b5aaba49-f865-3b55-e053-2995a90abcf4 id spl set id 9a6409d4-89f3-1ab8-e053-2995a90a3f1f set_id unii 27YLU75U4W openfda.unii unii C9642I91WL openfda.unii unii FXS1BY2PGL openfda.unii unii 6P669D8HQ8 openfda.unii unii 639KR60Q1Q openfda.unii unii 79Y1949PYO openfda.unii unii 6IO182RP7A openfda.unii unii WQZ3G9PF0H openfda.unii unii V0S6H36980 openfda.unii unii 2P299V784P openfda.unii unii VSW71SS07I openfda.unii unii U0NQ8555JD openfda.unii unii G6W4F0V8Z3 openfda.unii unii A49OS0F91S openfda.unii unii 9Z8D3HEM8L openfda.unii unii YHA2XLJ956 openfda.unii unii I76KB35JEV openfda.unii unii T7S323PKJS 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-feeding , ask a doctor before use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.