| Product NDC: | 63824-740 |
| Proprietary Name: | Cepacol |
| Non Proprietary Name: | Benzocaine and Dextromethorphan Hydrobromide |
| Active Ingredient(s): | 7.5; 5 mg/1; mg/1 & nbsp; Benzocaine and Dextromethorphan Hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63824-740 |
| Labeler Name: | Reckitt Benckiser LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110421 |
| Package NDC: | 63824-740-16 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (63824-740-16) > 8 LOZENGE in 1 BLISTER PACK |
| NDC Code | 63824-740-16 |
| Proprietary Name | Cepacol |
| Package Description | 2 BLISTER PACK in 1 CARTON (63824-740-16) > 8 LOZENGE in 1 BLISTER PACK |
| Product NDC | 63824-740 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine and Dextromethorphan Hydrobromide |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL |
| Start Marketing Date | 20110421 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Reckitt Benckiser LLC |
| Substance Name | BENZOCAINE; DEXTROMETHORPHAN HYDROBROMIDE |
| Strength Number | 7.5; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |