| Product NDC: | 55312-908 |
| Proprietary Name: | NightRelief Free |
| Non Proprietary Name: | acetaminophen,dextromethorphan HBr, doxylamine succinate |
| Active Ingredient(s): | 500; 15; 6.25 mg/15mL; mg/15mL; mg/15mL & nbsp; acetaminophen,dextromethorphan HBr, doxylamine succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55312-908 |
| Labeler Name: | Western Family Foods Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060501 |
| Package NDC: | 55312-908-30 |
| Package Description: | 177 mL in 1 BOTTLE (55312-908-30) |
| NDC Code | 55312-908-30 |
| Proprietary Name | NightRelief Free |
| Package Description | 177 mL in 1 BOTTLE (55312-908-30) |
| Product NDC | 55312-908 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen,dextromethorphan HBr, doxylamine succinate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20060501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Western Family Foods Inc |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 500; 15; 6.25 |
| Strength Unit | mg/15mL; mg/15mL; mg/15mL |
| Pharmaceutical Classes |