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day relief
day relief - 55312-818-38 - (Dextromethorphan HBr, Guaifenesin)
Drug Information of day relief
| Product NDC: | 55312-818 |
| Proprietary Name: | day relief |
| Non Proprietary Name: | Dextromethorphan HBr, Guaifenesin |
| Active Ingredient(s): | 10; 200 mg/15mL; mg/15mL & nbsp; Dextromethorphan HBr, Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of day relief
| Product NDC: | 55312-818 |
| Labeler Name: | Western Family Foods Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19970318 |
Package Information of day relief
| Package NDC: | 55312-818-38 |
| Package Description: | 296 mL in 1 BOTTLE (55312-818-38) |
NDC Information of day relief
| NDC Code | 55312-818-38 |
| Proprietary Name | day relief |
| Package Description | 296 mL in 1 BOTTLE (55312-818-38) |
| Product NDC | 55312-818 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan HBr, Guaifenesin |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19970318 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Western Family Foods Inc |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 10; 200 |
| Strength Unit | mg/15mL; mg/15mL |
| Pharmaceutical Classes |
