Product NDC: | 43611-002 |
Proprietary Name: | Melvita PROSUN SPF 15 Sun |
Non Proprietary Name: | TITANIUM DIOXIDE, ZINC OXIDE |
Active Ingredient(s): | 59.05; 120 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: | 43611-002 |
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: | 43611-002-00 |
Package Description: | 1 TUBE in 1 BOX (43611-002-00) > 75 mL in 1 TUBE |
NDC Code | 43611-002-00 |
Proprietary Name | Melvita PROSUN SPF 15 Sun |
Package Description | 1 TUBE in 1 BOX (43611-002-00) > 75 mL in 1 TUBE |
Product NDC | 43611-002 |
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 | 59.05; 120 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |