FDA.reportPublic FDA data

Aluminium phosphoricum

Manufacturer
Hahnemann Laboratories, Inc.
Effective date
2020-04-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:13:05

Label at a glance#

ProductAluminium phosphoricum
Active ingredientALUMINUM PHOSPHATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63545-892-012022-01-28C16284748780-1d6a99b39-f179-a426-e053-dadaa90af4c2a461ad57-6d79-74b2-e053-2a95a90a8aa2
63545-892-022022-01-28C16284748780-1d6a99b39-f179-a426-e053-dadaa90af4c2a461ad57-6d79-74b2-e053-2a95a90a8aa2
63545-892-032022-01-28C16284748780-1d6a99b39-f179-a426-e053-dadaa90af4c2a461ad57-6d79-74b2-e053-2a95a90a8aa2
63545-892-042022-01-28C16284748780-1d6a99b39-f179-a426-e053-dadaa90af4c2a461ad57-6d79-74b2-e053-2a95a90a8aa2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63545-892-01Aluminium phosphoricum200 in 1 VIAL, GLASSPELLET2001
63545-892-02Aluminium phosphoricum500 in 1 VIAL, GLASSPELLET5001
63545-892-03Aluminium phosphoricum3000 in 1 BOTTLE, GLASSPELLET30001
63545-892-04Aluminium phosphoricum10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63545-892ALUMINIUM PHOSPHORICUM PELLET [HAHNEMANN LABORATORIES, INC.]1Legacy NDC, 4 package rows20200429_a461ad57-6d79-74b2-e053-2a95a90a8aa2.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
63545-89263545-892-01, 63545-892-02, 63545-892-03, 63545-892-04

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
ALUMINUM PHOSPHATEF92V3S521OACTIB

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a461ad57-6d7a-74b2-e053-2a95a90a8aa2a461ad57-6d79-74b2-e053-2a95a90a8aa22020-04-28Exact identifier
spl id: a461ad57-6d7a-74b2-e053-2a95a90a8aa2
spl set id: a461ad57-6d79-74b2-e053-2a95a90a8aa2

Reported adverse events (FAERS/openFDA)#

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