FDA.reportPublic FDA data

Ammonium benzoicum

Product NDC
71919-040
Requested package NDC
71919-040-09
11-digit product format
719190040
Labeler code
71919
Product ID
71919-040_7e3ab47e-f1e6-f198-e053-2991aa0abdc8
Type
HUMAN OTC DRUG
Nonproprietary name
AMMONIUM BENZOATE
Dosage form
LIQUID
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2012-09-26
Marketing end
0000-00-00
Substance
AMMONIUM BENZOATE
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. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage71919-04071919-040-09DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71919-040-097191900400950 mL in 1 BOTTLE, GLASS (71919-040-09) 50 ml2012-09-260000-00-00NoNoCurrent