Abrotanum

Manufacturer
Hahnemann Laboratories, Inc.
Effective date
2022-07-26
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
full-release
Hydrated at
2026-06-01 02:17:51

Label at a glance#

ProductAbrotanum
Active ingredientARTEMISIA ABROTANUM FLOWERING TOP
Label structure1 sections

Label contents#

Full prescribing information#

Single label image contains content for sections 1-14.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Abrotanum 10M 1gAbrotanum 10M 1g

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63545-715-01Abrotanum200 in 1 VIAL, GLASSPELLET20011

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63545-715ABROTANUM PELLET [HAHNEMANN LABORATORIES, INC.]11Legacy NDC, 1 package rows20220728_9a00a36e-431f-fa51-e053-2995a90a16a6.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
63545-71563545-715-01

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
ARTEMISIA ABROTANUM FLOWERING TOPQG07G580U0ACTIB
SUCROSEC151H8M554IACT

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
e4c183b3-ae5a-3060-e053-2995a90a46169a00a36e-431f-fa51-e053-2995a90a16a62022-07-26Exact identifier
spl id: e4c183b3-ae5a-3060-e053-2995a90a4616
spl set id: 9a00a36e-431f-fa51-e053-2995a90a16a6

Reported adverse events (FAERS/openFDA)#

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