| Product NDC: | 51346-022 |
| Proprietary Name: | BEEVENOM BB |
| Non Proprietary Name: | TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
| Active Ingredient(s): | 2.8; 5.52; 1.56 g/40mL; g/40mL; g/40mL & nbsp; TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51346-022 |
| Labeler Name: | NATURE REPUBLIC CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120201 |
| Package NDC: | 51346-022-01 |
| Package Description: | 40 mL in 1 CARTON (51346-022-01) |
| NDC Code | 51346-022-01 |
| Proprietary Name | BEEVENOM BB |
| Package Description | 40 mL in 1 CARTON (51346-022-01) |
| Product NDC | 51346-022 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | NATURE REPUBLIC CO., LTD. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 2.8; 5.52; 1.56 |
| Strength Unit | g/40mL; g/40mL; g/40mL |
| Pharmaceutical Classes |