Product NDC: | 0799-0001 |
Proprietary Name: | Calmoseptine |
Non Proprietary Name: | Zinc Oxide and menthol |
Active Ingredient(s): | .44; 20.6 g/113g; g/113g & nbsp; Zinc Oxide and menthol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0799-0001 |
Labeler Name: | Calmoseptine Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19500801 |
Package NDC: | 0799-0001-02 |
Package Description: | 71 g in 1 TUBE (0799-0001-02) |
NDC Code | 0799-0001-02 |
Proprietary Name | Calmoseptine |
Package Description | 71 g in 1 TUBE (0799-0001-02) |
Product NDC | 0799-0001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Zinc Oxide and menthol |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 19500801 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Calmoseptine Inc. |
Substance Name | MENTHOL; ZINC OXIDE |
Strength Number | .44; 20.6 |
Strength Unit | g/113g; g/113g |
Pharmaceutical Classes |