Product NDC: | 13537-428 |
Proprietary Name: | LBEL |
Non Proprietary Name: | Zinc Oxide |
Active Ingredient(s): | .0157 g/mL & nbsp; Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13537-428 |
Labeler Name: | Ventura Corporation Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120210 |
Package NDC: | 13537-428-02 |
Package Description: | 1 TUBE in 1 BOX (13537-428-02) > 30 mL in 1 TUBE (13537-428-01) |
NDC Code | 13537-428-02 |
Proprietary Name | LBEL |
Package Description | 1 TUBE in 1 BOX (13537-428-02) > 30 mL in 1 TUBE (13537-428-01) |
Product NDC | 13537-428 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Zinc Oxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120210 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ventura Corporation Ltd. |
Substance Name | ZINC OXIDE |
Strength Number | .0157 |
Strength Unit | g/mL |
Pharmaceutical Classes |