| NDC Code | 55312-066-12 |
|---|
| Package Description | 355 mL in 1 BOTTLE, PLASTIC (55312-066-12) |
|---|
| Product NDC | 55312-066 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Dayrelief |
|---|
| Proprietary Name Suffix | Multi Symptom |
|---|
| Non-Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride |
|---|
| Dosage Form | LIQUID |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20150630 |
|---|
| End Marketing Date | 20191231 |
|---|
| Marketing Category Name | OTC MONOGRAPH FINAL |
|---|
| Application Number | part341 |
|---|
| Manufacturer | Western Family Foods, Inc. |
|---|
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 325; 10; 5 |
|---|
| Strength Unit | mg/15mL; mg/15mL; mg/15mL |
|---|