Aurum Plumbum

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-05-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:10:03

Label at a glance#

ProductAurum Plumbum
Active ingredientATROPA BELLADONNA, GOLD, LEAD
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Atropa belladonna ex herba (Nightshade) 10X, Aurum metallicum (Metallic gold) 10X, Plumbum mellitum (Lead with honey) 30X

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Organic sucrose

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AurumPlumbumPelletsAurumPlumbumPellets

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-1201-22026-01-29C16284748780-149896155-b041-586f-e063-e6dba90add90Aurum Plumbum

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1201-2Aurum Plumbum1350 in 1 BOTTLE, GLASSPELLET13503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1201AURUM PLUMBUM PELLET [URIEL PHARMACY INC.]3Legacy NDC, 1 package rows20180530_ae364e37-7ce0-412a-a9e8-29389ec4e201.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-120148951-1201-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
ATROPA BELLADONNAWQZ3G9PF0HACTIB
GOLD79Y1949PYOACTIB
LEAD2P299V784PACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
6d718999-1074-6467-e053-2991aa0afc25ae364e37-7ce0-412a-a9e8-29389ec4e2012018-05-30WarningsExact identifier
spl id: 6d718999-1074-6467-e053-2991aa0afc25
spl set id: ae364e37-7ce0-412a-a9e8-29389ec4e201

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.