| NDC Code | 61296-017-00 |
|---|
| Package Description | 1 BOTTLE, PUMP in 1 BOX (61296-017-00) / 50 mL in 1 BOTTLE, PUMP |
|---|
| Product NDC | 61296-017 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Biosolis Face Sunscreen Broadspectrum Spf50 |
|---|
| Non-Proprietary Name | Titanium Dioxide, Zinc Oxide |
|---|
| Dosage Form | CREAM |
|---|
| Usage | TOPICAL |
|---|
| Start Marketing Date | 20220107 |
|---|
| End Marketing Date | 20241231 |
|---|
| Marketing Category Name | OTC MONOGRAPH DRUG |
|---|
| Application Number | M020 |
|---|
| Manufacturer | Pro Vera SA |
|---|
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
|---|
| Strength | 100; 152 |
|---|
| Strength Unit | mg/mL; mg/mL |
|---|
| Pharmacy Classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
|---|