| Product NDC: | 37808-698 | 
| Proprietary Name: | rx act cough and sore throat | 
| Non Proprietary Name: | Acetaminophen, Dextromethorphan HBr | 
| Active Ingredient(s): | 500; 15 mg/15mL; mg/15mL & nbsp; Acetaminophen, Dextromethorphan HBr | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 37808-698 | 
| Labeler Name: | H E B | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20060828 | 
| Package NDC: | 37808-698-34 | 
| Package Description: | 237 mL in 1 BOTTLE (37808-698-34) | 
| NDC Code | 37808-698-34 | 
| Proprietary Name | rx act cough and sore throat | 
| Package Description | 237 mL in 1 BOTTLE (37808-698-34) | 
| Product NDC | 37808-698 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Acetaminophen, Dextromethorphan HBr | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 20060828 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | H E B | 
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 
| Strength Number | 500; 15 | 
| Strength Unit | mg/15mL; mg/15mL | 
| Pharmaceutical Classes |