FDA.reportPublic FDA data

Agnus castus

Manufacturer
Hahnemann Laboratories, Inc.
Effective date
2020-01-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:12:01

Label at a glance#

ProductAgnus castus
Active ingredientCHASTE TREE
Label structure1 sections

Label contents#

Full prescribing information#

Single label image contains content for sections 1-15.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Agnus castus 12C 5gAgnus castus 12C 5gAgnus castus 12C 30gAgnus castus 12C 30gAgnus castus 12C 100gAgnus castus 12C 100g

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63545-804-012022-01-28C16284748780-1d6a99b39-6c3f-a426-e053-dadaa90af4c29ba9df3c-0c9a-5538-e053-2995a90aa657
63545-804-022022-01-28C16284748780-1d6a99b39-6c3f-a426-e053-dadaa90af4c29ba9df3c-0c9a-5538-e053-2995a90aa657
63545-804-032022-01-28C16284748780-1d6a99b39-6c3f-a426-e053-dadaa90af4c29ba9df3c-0c9a-5538-e053-2995a90aa657

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63545-804-01Agnus castus200 in 1 VIAL, GLASSPELLET2001
63545-804-02Agnus castus1200 in 1 BOTTLE, GLASSPELLET12001
63545-804-03Agnus castus4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63545-804AGNUS CASTUS PELLET [HAHNEMANN LABORATORIES, INC.]1Legacy NDC, 3 package rows20200109_9ba9df3c-0c9a-5538-e053-2995a90aa657.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
63545-80463545-804-01, 63545-804-02, 63545-804-03

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
SUCROSEC151H8M554IACT
CHASTE TREE433OSF3U8AACTIB

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
9ba9df3c-0c9b-5538-e053-2995a90aa6579ba9df3c-0c9a-5538-e053-2995a90aa6572020-01-08Exact identifier
spl id: 9ba9df3c-0c9b-5538-e053-2995a90aa657
spl set id: 9ba9df3c-0c9a-5538-e053-2995a90aa657

Reported adverse events (FAERS/openFDA)#

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