Antiseptic - 51143-210-12 - (Eucalyptol)

Alphabetical Index


Drug Information of Antiseptic

Product NDC: 51143-210
Proprietary Name: Antiseptic
Non Proprietary Name: Eucalyptol
Active Ingredient(s): .092; .042; .06; .064    mL/100L; mL/100L; mL/100L; mL/100L & nbsp;   Eucalyptol
Administration Route(s): ORAL
Dosage Form(s): MOUTHWASH
Coding System: National Drug Codes(NDC)

Labeler Information of Antiseptic

Product NDC: 51143-210
Labeler Name: Onpoint, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part356
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20101019

Package Information of Antiseptic

Package NDC: 51143-210-12
Package Description: 1.5 L in 1 BOTTLE, PLASTIC (51143-210-12)

NDC Information of Antiseptic

NDC Code 51143-210-12
Proprietary Name Antiseptic
Package Description 1.5 L in 1 BOTTLE, PLASTIC (51143-210-12)
Product NDC 51143-210
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Eucalyptol
Dosage Form Name MOUTHWASH
Route Name ORAL
Start Marketing Date 20101019
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Onpoint, Inc
Substance Name EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL
Strength Number .092; .042; .06; .064
Strength Unit mL/100L; mL/100L; mL/100L; mL/100L
Pharmaceutical Classes

Complete Information of Antiseptic


General Information