| 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 |