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Badger SunScreen
Badger SunScreen - 51514-0232-1 - (Zinc Oxide)
Drug Information of Badger SunScreen
| Product NDC: | 51514-0232 |
| Proprietary Name: | Badger SunScreen |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | 10.6 mL/100mL & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Badger SunScreen
| Product NDC: | 51514-0232 |
| Labeler Name: | Autumn Harp, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120215 |
Package Information of Badger SunScreen
| Package NDC: | 51514-0232-1 |
| Package Description: | 87 mL in 1 TUBE (51514-0232-1) |
NDC Information of Badger SunScreen
| NDC Code | 51514-0232-1 |
| Proprietary Name | Badger SunScreen |
| Package Description | 87 mL in 1 TUBE (51514-0232-1) |
| Product NDC | 51514-0232 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120215 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Autumn Harp, Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | 10.6 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
