| Product NDC: | 27293-012 |
| Proprietary Name: | Oral Gel |
| Non Proprietary Name: | Benzocaine |
| Active Ingredient(s): | 20 g/100g & nbsp; Benzocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 27293-012 |
| Labeler Name: | Budpak Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100201 |
| Package NDC: | 27293-012-01 |
| Package Description: | 1 TUBE in 1 BOX (27293-012-01) > 14 g in 1 TUBE (27293-012-14) |
| NDC Code | 27293-012-01 |
| Proprietary Name | Oral Gel |
| Package Description | 1 TUBE in 1 BOX (27293-012-01) > 14 g in 1 TUBE (27293-012-14) |
| Product NDC | 27293-012 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Budpak Inc. |
| Substance Name | BENZOCAINE |
| Strength Number | 20 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |