Product NDC: | 51346-207 |
Proprietary Name: | PROVENCE TWO WAY PACT |
Non Proprietary Name: | Titanium Dioxide, OCTINOXATE, Zinc Oxide |
Active Ingredient(s): | .72; 1.39; .35 g/12g; g/12g; g/12g & nbsp; Titanium Dioxide, OCTINOXATE, Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51346-207 |
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: | 51346-207-01 |
Package Description: | 12 g in 1 CARTON (51346-207-01) |
NDC Code | 51346-207-01 |
Proprietary Name | PROVENCE TWO WAY PACT |
Package Description | 12 g in 1 CARTON (51346-207-01) |
Product NDC | 51346-207 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Titanium Dioxide, OCTINOXATE, Zinc Oxide |
Dosage Form Name | POWDER |
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 | .72; 1.39; .35 |
Strength Unit | g/12g; g/12g; g/12g |
Pharmaceutical Classes |