| 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 |