Product NDC: | 37000-399 |
Proprietary Name: | Dolce and Gabbana The Foundation |
Non Proprietary Name: | octinoxate and titanium dioxide |
Active Ingredient(s): | 4; 4 mg/mL; mg/mL & nbsp; octinoxate and titanium dioxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37000-399 |
Labeler Name: | Procter & Gamble Manufacturing Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110601 |
Package NDC: | 37000-399-15 |
Package Description: | 15 mL in 1 BOTTLE (37000-399-15) |
NDC Code | 37000-399-15 |
Proprietary Name | Dolce and Gabbana The Foundation |
Package Description | 15 mL in 1 BOTTLE (37000-399-15) |
Product NDC | 37000-399 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | octinoxate and titanium dioxide |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20110601 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Procter & Gamble Manufacturing Company |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 4; 4 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |