| Product NDC: | 76340-1201 |
| Proprietary Name: | Dr. Eslee Physical Sunscreen |
| Non Proprietary Name: | Zinc oxide |
| Active Ingredient(s): | .01248 g/g & nbsp; Zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76340-1201 |
| Labeler Name: | Ajou Medics Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130628 |
| Package NDC: | 76340-1201-1 |
| Package Description: | 60 g in 1 TUBE (76340-1201-1) |
| NDC Code | 76340-1201-1 |
| Proprietary Name | Dr. Eslee Physical Sunscreen |
| Package Description | 60 g in 1 TUBE (76340-1201-1) |
| Product NDC | 76340-1201 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130628 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ajou Medics Co., Ltd |
| Substance Name | ZINC OXIDE |
| Strength Number | .01248 |
| Strength Unit | g/g |
| Pharmaceutical Classes |