Mouth Rinse

Product NDC
51143-318
11-digit product format
511430318
Labeler code
51143
Product ID
51143-318_12fe4e58-941d-4fa3-abe9-88bee3823eea
Type
HUMAN OTC DRUG
Nonproprietary name
EUCALYPTOL, Menthol, Methyl salicylate, Thymol
Dosage form
MOUTHWASH
Route
ORAL
Labeler
Onpoint, Inc
Application
part356
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2009-07-27
Marketing end
0000-00-00
Substance
EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL
Active strength
1 mg/mL; mg/mL; mg/mL; mg/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 · 4 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct51143-318DDiscontinued by firm2026-08-03
excluded packagepackage51143-31851143-318-12DDiscontinued by firm2026-08-03
excluded packagepackage51143-31851143-318-77DDiscontinued by firm2026-08-03
excluded packagepackage51143-31851143-318-86DDiscontinued by firm2026-08-03

DailyMed Socrata Ingredients#