FDA.reportPublic FDA data

Aluminium metallicum

Manufacturer
Hahnemann Laboratories, Inc.
Effective date
2020-02-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:12:25

Label at a glance#

ProductAluminium metallicum
Active ingredientALUMINUM
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aluminium metallicum 100C 1gAluminium metallicum 100C 1gAluminium metallicum 100C 5gAluminium metallicum 100C 5gAluminium metallicum 100C 30gAluminium metallicum 100C 30gAluminium metallicum 100C 100gAluminium metallicum 100C 100g

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63545-869-012022-01-28C16284748780-1d6a99b39-52f2-a426-e053-dadaa90af4c29f5b4ec9-cd95-2389-e053-2995a90a99b5
63545-869-022022-01-28C16284748780-1d6a99b39-52f2-a426-e053-dadaa90af4c29f5b4ec9-cd95-2389-e053-2995a90a99b5
63545-869-032022-01-28C16284748780-1d6a99b39-52f2-a426-e053-dadaa90af4c29f5b4ec9-cd95-2389-e053-2995a90a99b5
63545-869-042022-01-28C16284748780-1d6a99b39-52f2-a426-e053-dadaa90af4c29f5b4ec9-cd95-2389-e053-2995a90a99b5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63545-869-01Aluminium metallicum200 in 1 VIAL, GLASSPELLET2001
63545-869-02Aluminium metallicum500 in 1 VIAL, GLASSPELLET5001
63545-869-03Aluminium metallicum3000 in 1 BOTTLE, GLASSPELLET30001
63545-869-04Aluminium metallicum10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63545-869ALUMINIUM METALLICUM PELLET [HAHNEMANN LABORATORIES, INC.]1Legacy NDC, 4 package rows20200225_9f5b4ec9-cd95-2389-e053-2995a90a99b5.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63545-86963545-869-01, 63545-869-02, 63545-869-03, 63545-869-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
ALUMINUMCPD4NFA903ACTIB

Source Document#

Source XML

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 · 4 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
A-5SUCROSEDNA Labs, Inc.8e63f697-26c1-4518-acd3-5ea72cfa27f72025-01-09WarningsName fallback
generic name: SUCROSE
Saccharum officinaleSUCROSEBoiron86d04552-b31a-0fcf-e053-2991aa0acecd2023-11-14Name fallback
generic name: SUCROSE
Saccharum officinaleSUCROSEBoiron86d05561-6f09-6f1f-e053-2a91aa0a4b982023-11-14Name fallback
generic name: SUCROSE
Saccharum officinaleSUCROSEBoiron6858f374-8549-4b00-e053-2991aa0a5c3c2023-02-20Name fallback
generic name: SUCROSE

Reported adverse events (FAERS/openFDA)#

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