| Product NDC: | 11509-0025 |
| Proprietary Name: | Cepacol Fizzlers |
| Non Proprietary Name: | benzocaine |
| Active Ingredient(s): | 6 mg/1 & nbsp; benzocaine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11509-0025 |
| Labeler Name: | Combe Incorporated |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090901 |
| Package NDC: | 11509-0025-1 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (11509-0025-1) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| NDC Code | 11509-0025-1 |
| Proprietary Name | Cepacol Fizzlers |
| Package Description | 2 BLISTER PACK in 1 CARTON (11509-0025-1) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| Product NDC | 11509-0025 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzocaine |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Combe Incorporated |
| Substance Name | BENZOCAINE |
| Strength Number | 6 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |