Flu Relief Therapy Day Time is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Rite Aid Corporation. The primary component is Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride.
| Product ID | 11822-2104_d8e61a79-c69e-4402-abec-2d52ae0c6f7b |
| NDC | 11822-2104 |
| Product Type | Human Otc Drug |
| Proprietary Name | Flu Relief Therapy Day Time |
| Generic Name | Acetaminophen, Dextromethorphan Hydrobromide,phenylephrine Hydrochloride |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2009-09-04 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | Rite Aid Corporation |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient Strength | 325 mg/15mL; mg/15mL; mg/15mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2009-09-04 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2009-09-04 |
| Marketing End Date | 2019-12-30 |
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 325 mg/15mL |
| SPL SET ID: | 01e78b45-869c-4472-bf94-ca478349ebb6 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 11822-2104 | Flu Relief Therapy Day Time | Acetaminophen, Dextromethorphan Hydrobromide,Phenylephrine Hydrochloride |
| 49580-0155 | Flu Relief Therapy Day Time | Theraflu Daytime |
| 68016-155 | Flu Relief Therapy Day Time | Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride |
| 82501-4661 | Cold and Flu Relief | Acetaminophen, Dextromethorphan Hydrobromide,Phenylephrine Hydrochloride |