| Product NDC: | 54305-331 |
| Proprietary Name: | DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 8.5 mg/1 & nbsp; MENTHOL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54305-331 |
| Labeler Name: | Ricola Ag |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110403 |
| Package NDC: | 54305-331-19 |
| Package Description: | 19 LOZENGE in 1 BAG (54305-331-19) |
| NDC Code | 54305-331-19 |
| Proprietary Name | DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC |
| Package Description | 19 LOZENGE in 1 BAG (54305-331-19) |
| Product NDC | 54305-331 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL |
| Start Marketing Date | 20110403 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ricola Ag |
| Substance Name | MENTHOL |
| Strength Number | 8.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |