| Product NDC: | 43611-001 |
| Proprietary Name: | Melvita PROSUN SPF 30 Sun |
| Non Proprietary Name: | TITANIUM DIOXIDE, ZINC OXIDE |
| Active Ingredient(s): | 93.05; 195 mg/mL; mg/mL & nbsp; TITANIUM DIOXIDE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43611-001 |
| Labeler Name: | Laboratoires M&L |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110912 |
| Package NDC: | 43611-001-00 |
| Package Description: | 1 TUBE in 1 BOX (43611-001-00) > 75 mL in 1 TUBE |
| NDC Code | 43611-001-00 |
| Proprietary Name | Melvita PROSUN SPF 30 Sun |
| Package Description | 1 TUBE in 1 BOX (43611-001-00) > 75 mL in 1 TUBE |
| Product NDC | 43611-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE, ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110912 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Laboratoires M&L |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 93.05; 195 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |