Product NDC: | 59567-001 |
Proprietary Name: | Capent |
Non Proprietary Name: | Zinc Oxide Lanolin |
Active Ingredient(s): | 15.5; 25 g/100g; g/100g & nbsp; Zinc Oxide Lanolin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59567-001 |
Labeler Name: | Laboratorios Columbia S.A. de C.V. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130301 |
Package NDC: | 59567-001-42 |
Package Description: | 42.5 g in 1 TUBE (59567-001-42) |
NDC Code | 59567-001-42 |
Proprietary Name | Capent |
Package Description | 42.5 g in 1 TUBE (59567-001-42) |
Product NDC | 59567-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Zinc Oxide Lanolin |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20130301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Laboratorios Columbia S.A. de C.V. |
Substance Name | LANOLIN; ZINC OXIDE |
Strength Number | 15.5; 25 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |