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#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63545-715-01 | 2024-01-30 | C162847 | 48780-1 | ba0f9c33-165f-a910-e053-dadaa90a0b85 | 9a00a36e-431f-fa51-e053-2995a90a16a6 |
| 63545-715-01 | 2022-07-27 | C162847 | 48780-1 | ba0f9c33-165f-a910-e053-dadaa90a0b85 | 9a00a36e-431f-fa51-e053-2995a90a16a6 |
| 63545-715-01 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-165f-a910-e053-dadaa90a0b85 | 9a00a36e-431f-fa51-e053-2995a90a16a6 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63545-715-01 | Abrotanum | 200 in 1 VIAL, GLASS | PELLET | 200 | 11 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Abrotanum
- ARTEMISIA ABROTANUM FLOWERING TOP
- SUCROSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63545-715 | 63545-715-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ARTEMISIA ABROTANUM FLOWERING TOP | QG07G580U0 | ACTIB |
| SUCROSE | C151H8M554 | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| e4c183b3-ae5a-3060-e053-2995a90a4616 | 9a00a36e-431f-fa51-e053-2995a90a16a6 | 2022-07-26 | e4c183b3-ae5a-3060-e053-2995a90a4616 9a00a36e-431f-fa51-e053-2995a90a16a6 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
