Antiseptic Mouth Rinse

Product NDC

51143-072

11-digit product format

511430072

Labeler code

51143

Product ID

51143-072_0d221c24-faa1-4eb3-8af2-1440377f59ce

Type

HUMAN OTC DRUG

Nonproprietary name

Eucalyptol

Dosage form

MOUTHWASH

Route

ORAL

Labeler

Onpoint, Inc

Application

part348

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