| Product NDC: | 59640-072 | 
| Proprietary Name: | Night Time Cherry | 
| Non Proprietary Name: | DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | 
| Active Ingredient(s): | 15; 135 mg/15mL; mg/5mL & nbsp; DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59640-072 | 
| Labeler Name: | H.E.B | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20090603 | 
| Package NDC: | 59640-072-01 | 
| Package Description: | 296 mL in 1 BOTTLE, PLASTIC (59640-072-01) | 
| NDC Code | 59640-072-01 | 
| Proprietary Name | Night Time Cherry | 
| Package Description | 296 mL in 1 BOTTLE, PLASTIC (59640-072-01) | 
| Product NDC | 59640-072 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 20090603 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | H.E.B | 
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE | 
| Strength Number | 15; 135 | 
| Strength Unit | mg/15mL; mg/5mL | 
| Pharmaceutical Classes |