| Product NDC: | 51325-100 |
| Proprietary Name: | Rejuvaderm Medispa sunscreen |
| Non Proprietary Name: | Octinoxate, Octisalate, Zinc oxide |
| Active Ingredient(s): | 9; 2.4; 9 mL/120mL; mL/120mL; mL/120mL & nbsp; Octinoxate, Octisalate, Zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51325-100 |
| Labeler Name: | Ellen H Frankle MD Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100801 |
| Package NDC: | 51325-100-01 |
| Package Description: | 120 mL in 1 TUBE (51325-100-01) |
| NDC Code | 51325-100-01 |
| Proprietary Name | Rejuvaderm Medispa sunscreen |
| Package Description | 120 mL in 1 TUBE (51325-100-01) |
| Product NDC | 51325-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, Zinc oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100801 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ellen H Frankle MD Inc |
| Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
| Strength Number | 9; 2.4; 9 |
| Strength Unit | mL/120mL; mL/120mL; mL/120mL |
| Pharmaceutical Classes |