| NDC Code | 52000-060-01 |
|---|
| Package Description | 1 TUBE in 1 CARTON (52000-060-01) > 14 g in 1 TUBE |
|---|
| Product NDC | 52000-060 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Oral Pain Relief |
|---|
| Non-Proprietary Name | Benzocaine And Benzalkonium Chloride |
|---|
| Dosage Form | GEL |
|---|
| Usage | TOPICAL |
|---|
| Start Marketing Date | 20201209 |
|---|
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
|---|
| Application Number | part356 |
|---|
| Manufacturer | Universal Distribution Center LLC |
|---|
| Substance Name | BENZALKONIUM CHLORIDE; BENZOCAINE |
|---|
| Strength | .01; .2 |
|---|
| Strength Unit | g/g; g/g |
|---|
| Pharmacy Classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
|---|