| Product NDC: | 55346-2903 |
| Proprietary Name: | Alpha-Caine |
| Non Proprietary Name: | Benzocaine |
| Active Ingredient(s): | 200 mg/g & nbsp; Benzocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55346-2903 |
| Labeler Name: | Dental Technologies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19991231 |
| Package NDC: | 55346-2903-1 |
| Package Description: | 30 g in 1 BOTTLE, PLASTIC (55346-2903-1) |
| NDC Code | 55346-2903-1 |
| Proprietary Name | Alpha-Caine |
| Package Description | 30 g in 1 BOTTLE, PLASTIC (55346-2903-1) |
| Product NDC | 55346-2903 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 19991231 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Dental Technologies, Inc. |
| Substance Name | BENZOCAINE |
| Strength Number | 200 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |