| Product NDC: | 0126-0082 |
| Proprietary Name: | Orabase Benzocaine |
| Non Proprietary Name: | Benzocaine |
| Active Ingredient(s): | 19.8 mg/g & nbsp; Benzocaine |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0126-0082 |
| Labeler Name: | Colgate Oral Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120801 |
| Package NDC: | 0126-0082-04 |
| Package Description: | 12 g in 1 TUBE (0126-0082-04) |
| NDC Code | 0126-0082-04 |
| Proprietary Name | Orabase Benzocaine |
| Package Description | 12 g in 1 TUBE (0126-0082-04) |
| Product NDC | 0126-0082 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20120801 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Colgate Oral Pharmaceuticals, Inc. |
| Substance Name | BENZOCAINE |
| Strength Number | 19.8 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |