DayClear SINUS PAIN AND PRESSURE is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Gm Pharmaceuticals, Inc. The primary component is Guaifenesin; Phenylephrine Hydrochloride; Choline Salicylate.
| Product ID | 58809-312_e18f4e87-1b11-4af7-a728-94ec25d3db77 |
| NDC | 58809-312 |
| Product Type | Human Otc Drug |
| Proprietary Name | DayClear SINUS PAIN AND PRESSURE |
| Generic Name | Choline Salicylate, Guaifenesin, Phenylephrine Hydrochloride |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2015-08-10 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | GM Pharmaceuticals, INC |
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE; CHOLINE SALICYLATE |
| Active Ingredient Strength | 200 mg/30mL; mg/30mL; mg/30mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2015-08-10 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-08-10 |
| Marketing End Date | 2018-12-10 |
| Ingredient | Strength |
|---|---|
| GUAIFENESIN | 200 mg/30mL |
| SPL SET ID: | 34a32f67-31a0-487d-e054-00144ff88e88 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |