Product NDC: | 55301-210 |
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) |
Product NDC: | 55301-210 |
Labeler Name: | Exchange Select |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101018 |
Package NDC: | 55301-210-86 |
Package Description: | 1 L in 1 BOTTLE, PLASTIC (55301-210-86) |
NDC Code | 55301-210-86 |
Proprietary Name | Antiseptic |
Package Description | 1 L in 1 BOTTLE, PLASTIC (55301-210-86) |
Product NDC | 55301-210 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Eucalyptol |
Dosage Form Name | MOUTHWASH |
Route Name | ORAL |
Start Marketing Date | 20101018 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Exchange Select |
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 |