| Product NDC: | 37808-977 | 
| Proprietary Name: | rx act nighttime | 
| Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate | 
| Active Ingredient(s): | 325; 15; 6.25 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | CAPSULE, LIQUID FILLED | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 37808-977 | 
| Labeler Name: | H E B | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20110610 | 
| Package NDC: | 37808-977-60 | 
| Package Description: | 2 BLISTER PACK in 1 CARTON (37808-977-60) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 
| NDC Code | 37808-977-60 | 
| Proprietary Name | rx act nighttime | 
| Package Description | 2 BLISTER PACK in 1 CARTON (37808-977-60) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 
| Product NDC | 37808-977 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate | 
| Dosage Form Name | CAPSULE, LIQUID FILLED | 
| Route Name | ORAL | 
| Start Marketing Date | 20110610 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | H E B | 
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE | 
| Strength Number | 325; 15; 6.25 | 
| Strength Unit | mg/1; mg/1; mg/1 | 
| Pharmaceutical Classes |