Sinus Relief is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Chain Drug Marketing Association. The primary component is Acetaminophen; Phenylephrine Hydrochloride.
| Product ID | 63868-972_7e5572b3-3d45-6b8b-e053-2991aa0a12f1 | 
| NDC | 63868-972 | 
| Product Type | Human Otc Drug | 
| Proprietary Name | Sinus Relief | 
| Generic Name | Acetaminophen And Phenylephrine Hydrochloride | 
| Dosage Form | Tablet, Coated | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2007-10-09 | 
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL | 
| Application Number | part341 | 
| Labeler Name | Chain Drug Marketing Association | 
| Substance Name | ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 
| Active Ingredient Strength | 325 mg/1; mg/1 | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2020-12-31 | 
| Marketing Start Date | 2007-10-09 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | OTC monograph final | 
| Application Number | part341 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2007-10-09 | 
| Marketing End Date | 2019-03-31 | 
| Ingredient | Strength | 
|---|---|
| ACETAMINOPHEN | 325 mg/1 | 
| SPL SET ID: | bf9b00c4-0f89-46c2-9651-abe6a4ab3fd3 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0363-0524 | Sinus Relief | Acetaminophen, Dextromethorphan HBR, Guaifenesin, Phenylephrine HCl | 
| 11822-5694 | Sinus Relief | Acetaminophen, Diphenhydramine HCl, Guaifenesin, Phenylephrine HCl | 
| 21130-502 | Sinus Relief | Acetaminophen, Phenylephrine HCl | 
| 21130-663 | Sinus Relief | Acetaminophen, Phenylephrine HCl | 
| 30142-011 | sinus relief | Acetaminophen, guaifenesin, phenylephrine HCl | 
| 30142-415 | sinus relief | acetaminophen, guaifenesin, phenylephrine hydrochloride, diphenhydramine hydrochloride | 
| 30142-616 | Sinus Relief | Acetaminophen, Diphenhydramine HCl, Guaifenesin, Phenylephrine HCl | 
| 30142-688 | Sinus Relief | Acetaminophen, guaifenesin, diphenhydramine HCl, phenylephrine HCl | 
| 30142-997 | Sinus Relief | Acetaminophen, guaifenesin, phenylephrine HCl | 
| 69842-569 | sinus relief | sinus relief | 
| 50441-0003 | Sinus Relief | Sinus Relief | 
| 57955-0134 | Sinus Relief | Sinus Relief | 
| 57955-5134 | Sinus Relief | Sinus Relief | 
| 59262-240 | Sinus Relief | Sinus Relief | 
| 59262-243 | Sinus Relief | Sinus Relief | 
| 60512-0015 | SINUS RELIEF | SINUS RELIEF | 
| 61727-335 | Sinus Relief | Sinus Relief | 
| 63868-972 | Sinus Relief | Sinus Relief | 
| 66579-0026 | Sinus Relief | Sinus Relief | 
| 46017-024 | Contac Cold and Flu | acetaminophen and phenylephrine hydrochloride | 
| 46017-021 | Contac Cold and Flu Day | acetaminophen and phenylephrine hydrochloride | 
| 33992-1100 | Daytime Sinus Relief | Acetaminophen and Phenylephrine Hydrochloride | 
| 36800-098 | Daytime Sinus Relief | Acetaminophen and Phenylephrine Hydrochloride | 
| 36800-911 | Pressure and Pain PE | ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE | 
| 41250-220 | Pressure and Pain PE | ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE | 
| 41250-623 | sinus and headache | ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE | 
| 41520-099 | Sinus Daytime | Acetaminophen and Phenylephrine Hydrochloride | 
| 36800-322 | Sinus plus Headache | ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE | 
| 41250-534 | Sinus plus Headache | ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE | 
| 41250-207 | sinus pressure and pain PE | ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE | 
| 36800-320 | Sinus Pressure plus Pain PE | ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE | 
| 37000-507 | Vicks Sinex | Acetaminophen and Phenylephrine Hydrochloride | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  SINUS RELIEF  78356033  not registered Dead/Abandoned | Stratford Ventures, Inc. 2004-01-22 | 
|  SINUS RELIEF  78090486  not registered Dead/Abandoned | Pincgold LLC 2001-10-27 |