FDA.reportPublic FDA data

Aluminum Acetate Astringent

Product NDC
51224-153
Requested package NDC
51224-153-24
11-digit product format
512240153
Labeler code
51224
Product ID
51224-153_a4b9d3a3-fe12-4313-922f-abc93f440e6c
Type
HUMAN OTC DRUG
Nonproprietary name
Calcium Acetate and Aluminum sulfate
Dosage form
POWDER, FOR SOLUTION
Route
TOPICAL
Labeler
TAGI Pharma Incorporated
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2011-06-15
Marketing end
0000-00-00
Substance
CALCIUM ACETATE; ALUMINUM SULFATE
Active strength
839 mg/2030mg; mg/2030mg
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage51224-15351224-153-24DDiscontinued by firm2026-08-11

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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51224-153-12EA - Each51224-1535d44d708-f3d0-4fce-a247-43c5e59de29912012-07-24
51224-153-24EA - Each51224-153ddadcdbf-7122-439a-a34f-4b489cf5f0f112012-07-24
51224-153-99EA - Each51224-153cac4fea4-7db4-455e-b348-f2ee4916b3a112012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Aluminum sulfateACTIVE INGREDIENT34S289N54EALUMINUM ACETATE ASTRINGENT (CALCIUM ACETATE AND ALUMINUM SULFATE) POWDER, FOR SOLUTION [TAGI PHARMA INCORPORATED]1
Calcium AcetateACTIVE INGREDIENTY882YXF34XALUMINUM ACETATE ASTRINGENT (CALCIUM ACETATE AND ALUMINUM SULFATE) POWDER, FOR SOLUTION [TAGI PHARMA INCORPORATED]1
Aluminum CationACTIVE MOIETY3XHB1D032BALUMINUM ACETATE ASTRINGENT (CALCIUM ACETATE AND ALUMINUM SULFATE) POWDER, FOR SOLUTION [TAGI PHARMA INCORPORATED]1
Calcium CationACTIVE MOIETY2M83C4R6ZBALUMINUM ACETATE ASTRINGENT (CALCIUM ACETATE AND ALUMINUM SULFATE) POWDER, FOR SOLUTION [TAGI PHARMA INCORPORATED]1
icodextrinINACTIVE INGREDIENT2NX48Z0A9GALUMINUM ACETATE ASTRINGENT (CALCIUM ACETATE AND ALUMINUM SULFATE) POWDER, FOR SOLUTION [TAGI PHARMA INCORPORATED]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51224-153-245122401532412 BOX in 1 CARTON (51224-153-24) > 12 POUCH in 1 BOX (51224-153-12) > 2030 mg in 1 POUCH (51224-153-99) 12 box2011-06-150000-00-00NoNoCurrent