FDA.reportPublic FDA data

Aluminium muriaticum

Manufacturer
Hahnemann Laboratories, Inc.
Effective date
2020-04-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:13:02

Label at a glance#

ProductAluminium muriaticum
Active ingredientALUMINUM CHLORIDE ANHYDROUS
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63545-876-012022-01-28C16284748780-1d6a99b39-d719-a426-e053-dadaa90af4c2a3707331-bea8-8401-e053-2995a90a118a
63545-876-022022-01-28C16284748780-1d6a99b39-d719-a426-e053-dadaa90af4c2a3707331-bea8-8401-e053-2995a90a118a
63545-876-032022-01-28C16284748780-1d6a99b39-d719-a426-e053-dadaa90af4c2a3707331-bea8-8401-e053-2995a90a118a
63545-876-042022-01-28C16284748780-1d6a99b39-d719-a426-e053-dadaa90af4c2a3707331-bea8-8401-e053-2995a90a118a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63545-876-01Aluminium muriaticum80 in 1 VIAL, GLASSPELLET801
63545-876-02Aluminium muriaticum200 in 1 VIAL, GLASSPELLET2001
63545-876-03Aluminium muriaticum1200 in 1 BOTTLE, GLASSPELLET12001
63545-876-04Aluminium muriaticum4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63545-876ALUMINIUM MURIATICUM PELLET [HAHNEMANN LABORATORIES, INC.]1Legacy NDC, 4 package rows20200417_a3707331-bea8-8401-e053-2995a90a118a.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
63545-87663545-876-01, 63545-876-02, 63545-876-03, 63545-876-04

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 CHLORIDE ANHYDROUSLIF1N9568YACTIB

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
a3707331-bea9-8401-e053-2995a90a118aa3707331-bea8-8401-e053-2995a90a118a2020-04-16Exact identifier
spl id: a3707331-bea9-8401-e053-2995a90a118a
spl set id: a3707331-bea8-8401-e053-2995a90a118a

Reported adverse events (FAERS/openFDA)#

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