FDA.reportPublic FDA data

Aluminium phosphoricum

Manufacturer
Hahnemann Laboratories, Inc.
Effective date
2020-04-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:13:04

Label at a glance#

ProductAluminium phosphoricum
Active ingredientALUMINUM PHOSPHATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aluminium phosphoricum 6C 5gAluminium phosphoricum 6C 5gAluminium phosphoricum 6C 30gAluminium phosphoricum 6C 30gAluminium phosphoricum 6C 100gAluminium phosphoricum 6C 100g

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63545-390-012022-01-28C16284748780-1d6a99b39-70ec-a426-e053-dadaa90af4c2a44d38e5-d78f-a34f-e053-2995a90a662e
63545-390-022022-01-28C16284748780-1d6a99b39-70ec-a426-e053-dadaa90af4c2a44d38e5-d78f-a34f-e053-2995a90a662e
63545-390-032022-01-28C16284748780-1d6a99b39-70ec-a426-e053-dadaa90af4c2a44d38e5-d78f-a34f-e053-2995a90a662e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63545-390-01Aluminium phosphoricum200 in 1 VIAL, GLASSPELLET2001
63545-390-02Aluminium phosphoricum1200 in 1 BOTTLE, GLASSPELLET12001
63545-390-03Aluminium phosphoricum4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63545-390ALUMINIUM PHOSPHORICUM PELLET [HAHNEMANN LABORATORIES, INC.]1Legacy NDC, 3 package rows20200428_a44d38e5-d78f-a34f-e053-2995a90a662e.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
63545-39063545-390-01, 63545-390-02, 63545-390-03

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
ALUMINUM PHOSPHATEF92V3S521OACTIB
SUCROSEC151H8M554IACT

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
a44d38e5-d790-a34f-e053-2995a90a662ea44d38e5-d78f-a34f-e053-2995a90a662e2020-04-27Exact identifier
spl id: a44d38e5-d790-a34f-e053-2995a90a662e
spl set id: a44d38e5-d78f-a34f-e053-2995a90a662e

Reported adverse events (FAERS/openFDA)#

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