Product NDC: | 51143-072 |
Proprietary Name: | Antiseptic Mouth Rinse |
Non Proprietary Name: | Eucalyptol |
Active Ingredient(s): | .092; .042; .06; .064 kg/100L; kg/100L; kg/100L; kg/100L & nbsp; Eucalyptol |
Administration Route(s): | ORAL |
Dosage Form(s): | MOUTHWASH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51143-072 |
Labeler Name: | Onpoint, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20090727 |
Package NDC: | 51143-072-86 |
Package Description: | 1 L in 1 BOTTLE, PLASTIC (51143-072-86) |
NDC Code | 51143-072-86 |
Proprietary Name | Antiseptic Mouth Rinse |
Package Description | 1 L in 1 BOTTLE, PLASTIC (51143-072-86) |
Product NDC | 51143-072 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Eucalyptol |
Dosage Form Name | MOUTHWASH |
Route Name | ORAL |
Start Marketing Date | 20090727 |
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 | kg/100L; kg/100L; kg/100L; kg/100L |
Pharmaceutical Classes |