FDA.reportPublic FDA data

Alumen

Product NDC
71919-033
11-digit product format
719190033
Labeler code
71919
Product ID
71919-033_99a4b884-7e0d-2efb-e053-2a95a90a393e
Type
HUMAN OTC DRUG
Nonproprietary name
POTASSIUM ALUM
Dosage form
LIQUID
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2010-09-08
Marketing end
0000-00-00
Substance
POTASSIUM ALUM
Active strength
30 [hp_C]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71919-033DDiscontinued by firm2026-07-31
excluded packagepackage71919-03371919-033-07DDiscontinued by firm2026-07-31
excluded packagepackage71919-03371919-033-08DDiscontinued by firm2026-07-31
excluded packagepackage71919-03371919-033-09DDiscontinued by firm2026-07-31
excluded packagepackage71919-03371919-033-10DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71919-033-077191900330715 mL in 1 VIAL, GLASS (71919-033-07) 15 ml2010-09-080000-00-00NoNoCurrent
71919-033-087191900330830 mL in 1 VIAL, GLASS (71919-033-08) 30 ml2010-09-080000-00-00NoNoCurrent
71919-033-097191900330950 mL in 1 BOTTLE, GLASS (71919-033-09) 50 ml2010-09-080000-00-00NoNoCurrent
71919-033-1071919003310100 mL in 1 BOTTLE, GLASS (71919-033-10) 100 ml2010-09-080000-00-00NoNoCurrent