| 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 |