FDA.reportPublic FDA data

Lithium Phosphoricum

Manufacturer
Hahnemann Laboratories, Inc.
Effective date
2016-12-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:27

Label at a glance#

ProductLithium Phosphoricum
Active ingredientLITHIUM PHOSPHATE
Label structure1 sections

Label contents#

Full prescribing information#

Single label image contains content for sections 1-17.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

imgimg

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 1280000Lith P.jpg, 44bcf4a2-11e4-19f0-e054-00144ff8d46c.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b3053bb1-353b-4a0b-bca5-28fe7228957cProduct name220250124
8ce6e144-236f-b7be-f690-f06e0c8c6bd3Product name220170725
f09af6ee-c6dd-d0ce-77ad-93508bcdacedProduct name420161205

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63545-661-012020-01-31C16284748780-19d75b9d0-6232-f424-e053-dadaa90a57ce44bcae39-2338-09ee-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63545-661-01Lithium Phosphoricum240 [hp_C] in 1 VIAL, GLASSPELLET2401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63545-661LITHIUM PHOSPHORICUM PELLET [HAHNEMANN LABORATORIES, INC.]1Legacy NDC, 1 package rows20161228_44bcae39-2338-09ee-e054-00144ff8d46c.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
63545-66163545-661-01

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
LITHIUM PHOSPHATE2QM4K05Q74ACTIB
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
44bcae39-2339-09ee-e054-00144ff8d46c44bcae39-2338-09ee-e054-00144ff8d46c2016-12-28Exact identifier
spl id: 44bcae39-2339-09ee-e054-00144ff8d46c
spl set id: 44bcae39-2338-09ee-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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