Absinthium
- Manufacturer
- Hahnemann Laboratories, Inc.
- Effective date
- 2025-01-09
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 12
- Source
- full-release
- Hydrated at
- 2026-06-01 02:30:35
Label at a glance#
ProductAbsinthium
Active ingredientWORMWOOD
Label structure1 sections
Label contents#
Full prescribing information#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63545-717-02 | 2022-07-27 | C162847 | 48780-1 | ba0f9c33-5d8a-a910-e053-dadaa90a0b85 | 9a00f4d8-3b08-9fbf-e053-2995a90ae26e |
| 63545-717-02 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-5d8a-a910-e053-dadaa90a0b85 | 9a00f4d8-3b08-9fbf-e053-2995a90ae26e |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63545-717-02 | Absinthium | 1200 in 1 BOTTLE, GLASS | PELLET | 1200 | 12 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Absinthium
- WORMWOOD
- SUCROSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63545-717 | 63545-717-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WORMWOOD | F84709P2XV | 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 |
|---|---|---|---|---|---|---|
| Absinthium | ABSINTHIUM | Hahnemann Laboratories, Inc. | 9a0126a4-483d-7e6b-e053-2a95a90a37d6 | 2025-01-09 | 63545-717 | |
| Absinthium | ABSINTHIUM | Hahnemann Laboratories, Inc. | 99f070ea-56e7-25a7-e053-2a95a90a7890 | 2025-01-09 | 63545-717 | |
| Absinthium | ABSINTHIUM | Hahnemann Laboratories, Inc. | 9a00f4d8-3b08-9fbf-e053-2995a90ae26e | 2025-01-09 | 63545-717-02 63545-717 63545071702 2b4a3e6f-e547-27d2-e063-6294a90ac352 9a00f4d8-3b08-9fbf-e053-2995a90ae26e |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
