Product NDC: | 10812-405 |
Proprietary Name: | Neutrogena |
Non Proprietary Name: | Titanium Dioxide and Zinc Oxide |
Active Ingredient(s): | 50; 30 mg/mL; mg/mL & nbsp; Titanium Dioxide and Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10812-405 |
Labeler Name: | Neutrogena Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101201 |
Package NDC: | 10812-405-01 |
Package Description: | 40 mL in 1 BOTTLE (10812-405-01) |
NDC Code | 10812-405-01 |
Proprietary Name | Neutrogena |
Package Description | 40 mL in 1 BOTTLE (10812-405-01) |
Product NDC | 10812-405 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Titanium Dioxide and Zinc Oxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20101201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Neutrogena Corporation |
Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 50; 30 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |