| Product NDC: | 51514-201 |
| Proprietary Name: | Badger SPF30 Unscented Sunscreen |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | 18.75 mL/100mL & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51514-201 |
| Labeler Name: | Autumn Harp, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111110 |
| Package NDC: | 51514-201-01 |
| Package Description: | 87 mL in 1 TUBE (51514-201-01) |
| NDC Code | 51514-201-01 |
| Proprietary Name | Badger SPF30 Unscented Sunscreen |
| Package Description | 87 mL in 1 TUBE (51514-201-01) |
| Product NDC | 51514-201 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20111110 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Autumn Harp, Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | 18.75 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |