Product NDC: | 63730-292 |
Proprietary Name: | Diamond White Brightening Shield Treatment Cream |
Non Proprietary Name: | Ethylhexyl Methoxycinnamate (Octinoxate), Titanium Dioxide, Zinc Oxide |
Active Ingredient(s): | 2.4; .9; 5.7 mg/30mL; mg/30mL; mg/30mL & nbsp; Ethylhexyl Methoxycinnamate (Octinoxate), Titanium Dioxide, Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63730-292 |
Labeler Name: | Natura Bisse International |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130125 |
Package NDC: | 63730-292-01 |
Package Description: | 30 mL in 1 BOX (63730-292-01) |
NDC Code | 63730-292-01 |
Proprietary Name | Diamond White Brightening Shield Treatment Cream |
Package Description | 30 mL in 1 BOX (63730-292-01) |
Product NDC | 63730-292 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ethylhexyl Methoxycinnamate (Octinoxate), Titanium Dioxide, Zinc Oxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130125 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Natura Bisse International |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 2.4; .9; 5.7 |
Strength Unit | mg/30mL; mg/30mL; mg/30mL |
Pharmaceutical Classes |