| 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 |