Product NDC: | 54151-101 |
Proprietary Name: | Ingenue |
Non Proprietary Name: | Zinc Oxide |
Active Ingredient(s): | 14.5 mg/mL & nbsp; Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54151-101 |
Labeler Name: | Ingenue, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120615 |
Package NDC: | 54151-101-26 |
Package Description: | 1 TUBE in 1 BOX (54151-101-26) > 50 mL in 1 TUBE |
NDC Code | 54151-101-26 |
Proprietary Name | Ingenue |
Package Description | 1 TUBE in 1 BOX (54151-101-26) > 50 mL in 1 TUBE |
Product NDC | 54151-101 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Zinc Oxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120615 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ingenue, LLC |
Substance Name | ZINC OXIDE |
Strength Number | 14.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |