Home NDC 63545-900-03 Aluminium sulphuricum
Product NDC 63545-900
Requested package NDC 63545-900-03
11-digit product format 635450900
Labeler code 63545
Product ID 63545-900_2b4a9c74-d8fd-54ab-e063-6294a90a6799
Type HUMAN OTC DRUG
Nonproprietary name Aluminium sulphuricum
Dosage form PELLET
Route ORAL
Labeler Hahnemann Laboratories, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-04-29
Substance ALUMINUM SULFATE
Active strength 100 [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 2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 63545-900 63545-900-03 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 63545-900 63545-900-03 I Inactivated by FDA excluded / ndc_excluded.zip 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 63545-900 63545-900-03 I Inactivated by FDA excluded / ndc_excluded.zip bd6a592717d7…303034d00443…
Additional Listing Data#
Finished product Yes
Brand name base Aluminium sulphuricum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM SULFATE 100 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 34S289N54E 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 63545-900-01 Aluminium sulphuricum 200 in 1 VIAL, GLASS PELLET 200 3 63545-900-02 Aluminium sulphuricum 500 in 1 VIAL, GLASS PELLET 500 3 63545-900-03 Aluminium sulphuricum 3000 in 1 BOTTLE, GLASS PELLET 3000 3 63545-900-04 Aluminium sulphuricum 10000 in 1 BOTTLE, GLASS PELLET 10000 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63545-900 ALUMINIUM SULPHURICUM PELLET [HAHNEMANN LABORATORIES, INC.] 3 Current NDC, Legacy NDC, 4 package rows 20250112_a474ba15-34a5-f07e-e053-2995a90a61ca.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 · 1 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 63545-900-03 63545090003 3000 PELLET in 1 BOTTLE, GLASS (63545-900-03) 3000 pellet 2020-04-29 0000-00-00 No No Current