Anticavity

Product NDC
51143-966
11-digit product format
511430966
Labeler code
51143
Product ID
51143-966_61ae85f9-238c-40bc-b2fc-bc335d78f3af
Type
HUMAN OTC DRUG
Nonproprietary name
Sdoium Fluoride
Dosage form
MOUTHWASH
Route
ORAL
Labeler
Onpoint, Inc
Application
part355
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2012-03-21
Marketing end
0000-00-00
Substance
SODIUM FLUORIDE
Active strength
0 mL/100L
NDC exclude flag
E
Listing certified through
2018-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct51143-966DDiscontinued by firm2026-08-03
excluded packagepackage51143-96651143-966-86DDiscontinued by firm2026-08-03

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51143-966-862025-02-25C16284748780-19d75b9d0-8a76-f424-e053-dadaa90a57ceDrug Facts
51143-966-862020-01-31C16284748780-19d75b9d0-8a76-f424-e053-dadaa90a57ceDrug Facts

DailyMed Socrata Ingredients#