Abrotanum

Manufacturer: Hahnemann Laboratories, Inc.
Effective date: 2025-01-09
Label type: HUMAN OTC DRUG LABEL
Version: 11
Source: full-release
Hydrated at: 2026-06-01 02:30:34

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 1M 1g

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63545-714-01	2022-07-27	C162847	48780-1	ba0f9c33-5396-a910-e053-dadaa90a0b85	9a0036e9-0c43-6cef-e053-2995a90a7298
63545-714-01	2021-01-29	C162847	48780-1	ba0f9c33-5396-a910-e053-dadaa90a0b85	9a0036e9-0c43-6cef-e053-2995a90a7298

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63545-714-01	Abrotanum	200 in 1 VIAL, GLASS	PELLET	200		11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63545-714	ABROTANUM PELLET [HAHNEMANN LABORATORIES, INC.]	11	Current NDC, Legacy NDC, 1 package rows	20250112_9a0036e9-0c43-6cef-e053-2995a90a7298.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Abrotanum
ARTEMISIA ABROTANUM FLOWERING TOP
SUCROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63545-714	63545-714-01

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
Name	UNII	Kind
ARTEMISIA ABROTANUM FLOWERING TOP	QG07G580U0	ACTIB
SUCROSE	C151H8M554	IACT

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 · 4 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Join
Abrotanum	ABROTANUM	Hahnemann Laboratories, Inc.	9a0036e9-0c43-6cef-e053-2995a90a7298	2025-01-09	Exact identifier ndc (package): 63545-714-01 ndc (product): 63545-714 ndc11 (package): 63545071401 spl id: 2b4a1f65-5ba8-16e6-e063-6394a90afb58 spl set id: 9a0036e9-0c43-6cef-e053-2995a90a7298
Abrotanum	ABROTANUM	Hahnemann Laboratories, Inc.	9a007e04-eaf4-fc06-e053-2995a90a82d2	2025-01-09	Exact identifier ndc (product): 63545-714
Abrotanum	ABROTANUM	Hahnemann Laboratories, Inc.	9a0032c4-afd5-4eba-e053-2995a90ad301	2025-01-09	Exact identifier ndc (product): 63545-714
Abrotanum	ABROTANUM	Hahnemann Laboratories, Inc.	9a00719d-eaf6-d8c3-e053-2995a90ac960	2025-01-09	Exact identifier ndc (product): 63545-714

Reported adverse events (FAERS/openFDA)#

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