FDA.reportPublic FDA data

Hemoban

Product NDC
0699-1081
Requested package NDC
0699-1081-01
11-digit product format
006991081
Labeler code
0699
Product ID
0699-1081_8a5fff25-5e0a-4ebc-91db-792171cc3f1f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Aluminum Chloride
Dosage form
SOLUTION
Route
DENTAL
Labeler
Dentsply LLC, Professional Division Trading as "Sultan Healthcare"
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
1963-02-19
Marketing end
0000-00-00
Substance
ALUMINUM CHLORIDE ANHYDROUS
Active strength
250 mg/g
NDC exclude flag
No
Listing certified through
2023-12-31
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 packagepackage0699-10810699-1081-01DDiscontinued by firm2026-09-14

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…

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0699-1081-012020-08-19C16284748780-1ab0e2407-320e-f274-e053-dbdaa90a6471Hemoban
0699-1081-012020-07-22C16284748780-1ab0e2407-320e-f274-e053-dbdaa90a6471Hemoban

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Aluminum Chloride AnhydrousACTIVE INGREDIENTLIF1N9568YHEMOBAN (ALUMINUM CHLORIDE) SOLUTION [DENTSPLY LLC, PROFESSIONAL DIVISION TRADING AS "SULTAN HEALTHCARE"]2
Aluminum CationACTIVE MOIETY3XHB1D032BHEMOBAN (ALUMINUM CHLORIDE) SOLUTION [DENTSPLY LLC, PROFESSIONAL DIVISION TRADING AS "SULTAN HEALTHCARE"]2
WaterINACTIVE INGREDIENT059QF0KO0RHEMOBAN (ALUMINUM CHLORIDE) SOLUTION [DENTSPLY LLC, PROFESSIONAL DIVISION TRADING AS "SULTAN HEALTHCARE"]2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0699-1081-010069910810135.6 g in 1 BOTTLE, GLASS (0699-1081-01) 35.6 g1963-02-190000-00-00NoNoCurrent