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Night Relief Free
Night Relief Free - 55312-041-43 - (acetaminophen, dextromethorphan hydrobromide and doxylamine succinate)
Drug Information of Night Relief Free
| Product NDC: | 55312-041 |
| Proprietary Name: | Night Relief Free |
| Non Proprietary Name: | acetaminophen, dextromethorphan hydrobromide and doxylamine succinate |
| Active Ingredient(s): | 500; 15; 6.25 mg/15mL; mg/15mL; mg/15mL & nbsp; acetaminophen, dextromethorphan hydrobromide and doxylamine succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Night Relief Free
| Product NDC: | 55312-041 |
| Labeler Name: | Western Family Foods inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090915 |
Package Information of Night Relief Free
| Package NDC: | 55312-041-43 |
| Package Description: | 473 mL in 1 BOTTLE (55312-041-43) |
NDC Information of Night Relief Free
| NDC Code | 55312-041-43 |
| Proprietary Name | Night Relief Free |
| Package Description | 473 mL in 1 BOTTLE (55312-041-43) |
| Product NDC | 55312-041 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen, dextromethorphan hydrobromide and doxylamine succinate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20090915 |
| 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 |
