Product NDC: | 50145-222 |
Proprietary Name: | Hipoglos |
Non Proprietary Name: | Zinc Oxide and Lanolin |
Active Ingredient(s): | 15; 15 g/100g; g/100g & nbsp; Zinc Oxide and Lanolin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50145-222 |
Labeler Name: | Laboratorios Andromaco S.A. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101103 |
Package NDC: | 50145-222-02 |
Package Description: | 1 TUBE in 1 CARTON (50145-222-02) > 100 g in 1 TUBE |
NDC Code | 50145-222-02 |
Proprietary Name | Hipoglos |
Package Description | 1 TUBE in 1 CARTON (50145-222-02) > 100 g in 1 TUBE |
Product NDC | 50145-222 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Zinc Oxide and Lanolin |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20101103 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Laboratorios Andromaco S.A. |
Substance Name | LANOLIN; ZINC OXIDE |
Strength Number | 15; 15 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |