FDA.reportPublic FDA data

Aluminium sulphuricum

Manufacturer
Hahnemann Laboratories, Inc.
Effective date
2020-04-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:13:06

Label at a glance#

ProductAluminium sulphuricum
Active ingredientALUMINUM SULFATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63545-899-012022-01-28C16284748780-1d6a99b39-3be3-a426-e053-dadaa90af4c2a4748bfb-8d12-dea8-e053-2995a90acdce
63545-899-022022-01-28C16284748780-1d6a99b39-3be3-a426-e053-dadaa90af4c2a4748bfb-8d12-dea8-e053-2995a90acdce
63545-899-032022-01-28C16284748780-1d6a99b39-3be3-a426-e053-dadaa90af4c2a4748bfb-8d12-dea8-e053-2995a90acdce
63545-899-042022-01-28C16284748780-1d6a99b39-3be3-a426-e053-dadaa90af4c2a4748bfb-8d12-dea8-e053-2995a90acdce

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63545-899-01Aluminium sulphuricum80 in 1 VIAL, GLASSPELLET801
63545-899-02Aluminium sulphuricum200 in 1 VIAL, GLASSPELLET2001
63545-899-03Aluminium sulphuricum3000 in 1 BOTTLE, GLASSPELLET30001
63545-899-04Aluminium sulphuricum10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63545-899ALUMINIUM SULPHURICUM PELLET [HAHNEMANN LABORATORIES, INC.]1Legacy NDC, 4 package rows20200430_a4748bfb-8d12-dea8-e053-2995a90acdce.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63545-89963545-899-01, 63545-899-02, 63545-899-03, 63545-899-04

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 SULFATE34S289N54EACTIB

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
a4748bfb-8d13-dea8-e053-2995a90acdcea4748bfb-8d12-dea8-e053-2995a90acdce2020-04-29Exact identifier
spl id: a4748bfb-8d13-dea8-e053-2995a90acdce
spl set id: a4748bfb-8d12-dea8-e053-2995a90acdce

Reported adverse events (FAERS/openFDA)#

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