Home NDC 63545-717-02 Absinthium
Product NDC 63545-717
Requested package NDC 63545-717-02
11-digit product format 635450717
Labeler code 63545
Product ID 63545-717_2b4a2c07-24cf-ac03-e063-6394a90a3535
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 12 [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 date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 63545-717 63545-717-02 I Inactivated by FDA excluded / ndc_excluded.zip 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 63545-717 63545-717-02 I Inactivated by FDA excluded / ndc_excluded.zip bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 63545-717 63545-717-02 I Inactivated by FDA excluded / ndc_excluded.zip 8dfbde2a14a4…c9ff85d89658…
Additional Listing Data#
Finished product Yes
Brand name base Absinthium
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WORMWOOD 12 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F84709P2XV Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63545-717-02 Absinthium 1200 in 1 BOTTLE, GLASS PELLET 1200 12 63545-717-03 Absinthium 4000 in 1 BOTTLE, GLASS PELLET 4000 12 63545-717-01 Absinthium 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 63545-717 ABSINTHIUM PELLET [HAHNEMANN LABORATORIES, INC.] 12 Current NDC, Legacy NDC, 1 package rows 20250112_9a00f4d8-3b08-9fbf-e053-2995a90ae26e.zip 63545-717 ABSINTHIUM PELLET [HAHNEMANN LABORATORIES, INC.] 12 Current NDC, Legacy NDC, 1 package rows 20250112_9a0126a4-483d-7e6b-e053-2a95a90a37d6.zip 63545-717 ABSINTHIUM PELLET [HAHNEMANN LABORATORIES, INC.] 11 Current NDC, Legacy NDC, 1 package rows 20250112_99f070ea-56e7-25a7-e053-2a95a90a7890.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 · 3 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63545-717-02 63545071702 1200 PELLET in 1 BOTTLE, GLASS (63545-717-02) 1200 pellet 2019-12-18 0000-00-00 No No Current