FDA.reportPublic FDA data

Absinthium

Product NDC
63545-721
Requested package NDC
63545-721-03
11-digit product format
635450721
Labeler code
63545
Product ID
63545-721_2b4a1f65-5baa-16e6-e063-6394a90afb58
Type
HUMAN OTC DRUG
Nonproprietary name
Absinthium
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-12-18
Substance
WORMWOOD
Active strength
500 [hp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 3 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage63545-72163545-721-03IInactivated by FDAexcluded / ndc_excluded.zip86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage63545-72163545-721-03IInactivated by FDAexcluded / ndc_excluded.zipbd6a592717d7…303034d00443…
2021-12-27 23:28 UTC · source 2021-12-27excluded packagepackage63545-72163545-721-03IInactivated by FDAexcluded / ndc_excluded.zip8dfbde2a14a4…c9ff85d89658…

Additional Listing Data#

Finished product
Yes
Brand name base
Absinthium
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
WORMWOOD500 [hp_C]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F84709P2XVInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9a03e936-b005-6dec-e053-2a95a90ad14aAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Indexing SPL table
NDCEffectiveIndexing SPLRelated label
63545-721-012022-07-26ba0f9c33-16bc-a910-e053-dadaa90a0b859a03c1f7-098c-035d-e053-2a95a90a1fef
63545-721-022022-07-26ba0f9c33-16b9-a910-e053-dadaa90a0b859a037f09-4092-714f-e053-2a95a90a52f6
63545-721-032022-07-26ba0f9c33-5dde-a910-e053-dadaa90a0b859a03e936-b005-6dec-e053-2a95a90ad14a
63545-721-042022-07-26ba0f9c33-5dc6-a910-e053-dadaa90a0b859a03e936-b01a-6dec-e053-2a95a90ad14a
63545-721-012021-01-29ba0f9c33-16bc-a910-e053-dadaa90a0b859a03c1f7-098c-035d-e053-2a95a90a1fef
63545-721-022021-01-29ba0f9c33-16b9-a910-e053-dadaa90a0b859a037f09-4092-714f-e053-2a95a90a52f6
63545-721-032021-01-29ba0f9c33-5dde-a910-e053-dadaa90a0b859a03e936-b005-6dec-e053-2a95a90ad14a
63545-721-042021-01-29ba0f9c33-5dc6-a910-e053-dadaa90a0b859a03e936-b01a-6dec-e053-2a95a90ad14a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63545-721-04Absinthium10000 in 1 BOTTLE, GLASSPELLET1000019
63545-721-02Absinthium500 in 1 VIAL, GLASSPELLET50018
63545-721-03Absinthium3000 in 1 VIAL, GLASSPELLET300018
63545-721-01Absinthium200 in 1 VIAL, GLASSPELLET20017

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63545-721ABSINTHIUM PELLET [HAHNEMANN LABORATORIES, INC.]19Current NDC, Legacy NDC, 1 package rows20250112_9a03e936-b01a-6dec-e053-2a95a90ad14a.zip
63545-721ABSINTHIUM PELLET [HAHNEMANN LABORATORIES, INC.]18Current NDC, Legacy NDC, 1 package rows20250112_9a037f09-4092-714f-e053-2a95a90a52f6.zip
63545-721ABSINTHIUM PELLET [HAHNEMANN LABORATORIES, INC.]18Current NDC, Legacy NDC, 1 package rows20250112_9a03e936-b005-6dec-e053-2a95a90ad14a.zip
63545-721ABSINTHIUM PELLET [HAHNEMANN LABORATORIES, INC.]17Current NDC, Legacy NDC, 1 package rows20250112_9a03c1f7-098c-035d-e053-2a95a90a1fef.zip

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AbsinthiumABSINTHIUMHahnemann Laboratories, Inc.9a03e936-b005-6dec-e053-2a95a90ad14a2025-01-09Exact identifier
ndc (package): 63545-721-03
ndc (product): 63545-721
ndc11 (package): 63545072103
AbsinthiumABSINTHIUMHahnemann Laboratories, Inc.9a037f09-4092-714f-e053-2a95a90a52f62025-01-09Exact identifier
ndc (product): 63545-721
AbsinthiumABSINTHIUMHahnemann Laboratories, Inc.9a03e936-b01a-6dec-e053-2a95a90ad14a2025-01-09Exact identifier
ndc (product): 63545-721
AbsinthiumABSINTHIUMHahnemann Laboratories, Inc.9a03c1f7-098c-035d-e053-2a95a90a1fef2025-01-09Exact identifier
ndc (product): 63545-721

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63545-721-03635450721033000 PELLET in 1 VIAL, GLASS (63545-721-03) 3000 pellet2019-12-180000-00-00NoNoCurrent