FDA.reportPublic FDA data

Benzoicum Ac

Product NDC
68428-254
Requested package NDC
68428-254-12
11-digit product format
684280254
Labeler code
68428
Product ID
68428-254_6c7dcc74-a260-27b8-e053-2991aa0a9813
Type
HUMAN OTC DRUG
Nonproprietary name
BENZOIC ACID
Dosage form
PELLET
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2010-04-29
Marketing end
0000-00-00
Substance
BENZOIC ACID
Active strength
30 [hp_C]/1
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 packagepackage68428-25468428-254-12DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68428-254-1268428025412600 PELLET in 1 BOTTLE, GLASS (68428-254-12) 600 pellet2010-04-290000-00-00NoNoCurrent