Product NDC: | 51346-202 |
Proprietary Name: | PROVENCE FOUNDATION |
Non Proprietary Name: | Titanium Dioxide, OCTINOXATE, Zinc Oxide |
Active Ingredient(s): | 1.4; 3.65; .34 mg/35mL; mg/35mL; mg/35mL & nbsp; Titanium Dioxide, OCTINOXATE, Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51346-202 |
Labeler Name: | NATURE REPUBLIC CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130201 |
Package NDC: | 51346-202-01 |
Package Description: | 35 mL in 1 CARTON (51346-202-01) |
NDC Code | 51346-202-01 |
Proprietary Name | PROVENCE FOUNDATION |
Package Description | 35 mL in 1 CARTON (51346-202-01) |
Product NDC | 51346-202 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Titanium Dioxide, OCTINOXATE, Zinc Oxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | NATURE REPUBLIC CO., LTD. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 1.4; 3.65; .34 |
Strength Unit | mg/35mL; mg/35mL; mg/35mL |
Pharmaceutical Classes |