Product NDC: | 12090-0032 |
Proprietary Name: | Lantiseptic |
Non Proprietary Name: | MENTHOL, CALAMINE, ZINC OXIDE |
Active Ingredient(s): | 20; 4.5; 180 mg/g; mg/g; mg/g & nbsp; MENTHOL, CALAMINE, ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 12090-0032 |
Labeler Name: | Summit Industries, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091230 |
Package NDC: | 12090-0032-4 |
Package Description: | 113 g in 1 TUBE (12090-0032-4) |
NDC Code | 12090-0032-4 |
Proprietary Name | Lantiseptic |
Package Description | 113 g in 1 TUBE (12090-0032-4) |
Product NDC | 12090-0032 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | MENTHOL, CALAMINE, ZINC OXIDE |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20091230 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Summit Industries, Inc. |
Substance Name | FERRIC OXIDE RED; MENTHOL; ZINC OXIDE |
Strength Number | 20; 4.5; 180 |
Strength Unit | mg/g; mg/g; mg/g |
Pharmaceutical Classes |