| Product NDC: | 37808-335 | 
| Proprietary Name: | night time | 
| Non Proprietary Name: | Acetaminophen, Dextromethorphan HBr, Doxylamine succinate | 
| Active Ingredient(s): | 650; 30; 12.5 mg/30mL; mg/30mL; mg/30mL & nbsp; Acetaminophen, Dextromethorphan HBr, Doxylamine succinate | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 37808-335 | 
| Labeler Name: | H E B | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20130207 | 
| Package NDC: | 37808-335-40 | 
| Package Description: | 355 mL in 1 BOTTLE (37808-335-40) | 
| NDC Code | 37808-335-40 | 
| Proprietary Name | night time | 
| Package Description | 355 mL in 1 BOTTLE (37808-335-40) | 
| Product NDC | 37808-335 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Acetaminophen, Dextromethorphan HBr, Doxylamine succinate | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 20130207 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | H E B | 
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE | 
| Strength Number | 650; 30; 12.5 | 
| Strength Unit | mg/30mL; mg/30mL; mg/30mL | 
| Pharmaceutical Classes |