Cold Relief Maximum Strength / Day Time is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Dolgencorp, Llc. The primary component is Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride.
| Product ID | 55910-470_3690946e-f0ad-4f72-b2dc-f3e199a7b5a8 |
| NDC | 55910-470 |
| Product Type | Human Otc Drug |
| Proprietary Name | Cold Relief Maximum Strength / Day Time |
| Generic Name | Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2005-07-15 |
| Marketing End Date | 2023-11-17 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | DOLGENCORP, LLC |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient Strength | 325 mg/1; mg/1; mg/1 |
| NDC Exclude Flag | N |
| Marketing Start Date | 2005-07-15 |
| Marketing End Date | 2023-11-17 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2005-07-15 |
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 325 mg/1 |
| SPL SET ID: | 9c533ef9-363b-4d8e-8c5c-3298fc74c5b5 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 55910-470 | Cold Relief Maximum Strength / Day Time | Cold Relief Maximum Strength / Day Time |
| 0113-7994 | basic care daytime cold and flu | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| 0113-7690 | basic care severe cold and flu | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| 0363-0560 | Cold | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| 0363-0666 | Cold and Flu | acetaminophen, dextromethorphan Hbr, Phenylephrine HCl |
| 0363-6590 | Cold and Flu | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| 0363-7301 | Cold and Flu | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| 0067-2077 | COMTREX | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| 0363-0656 | Daytime Cold and Flu Relief | acetaminophen, dextromethorphan Hbr, Phenylephrine HCl |
| 0113-0064 | Good Sense Cold Max | Acetaminophen, Dextromethorphan hbr, Phenylephrine hcl |
| 0113-0656 | Good Sense Daytime | acetaminophen, dextromethorphan Hbr, Phenylephrine HCl |
| 0113-0994 | good sense daytime | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| 0113-0023 | good sense multi symptom flu and severe cold | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| 0363-5470 | Multi Symptom Wal Flu Severe Cold | ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl |
| 0067-6426 | THERAFLU | ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl |
| 0067-8127 | Theraflu ExpressMax | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| 0067-8136 | Theraflu ExpressMax | acetaminophen, dextromethorphan HBr, phenylephrine HCl |
| 0363-8319 | wal flu severe cold | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| 0363-5110 | Wal-Phed | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() COLD RELIEF 86711991 5125993 Live/Registered |
T.R.P. Company, Inc. 2015-07-31 |
![]() COLD RELIEF 75909317 not registered Dead/Abandoned |
Super Ice Corporation 2000-02-03 |
![]() COLD RELIEF 73537444 1397539 Dead/Cancelled |
SUPER ICE CORPORATION 1985-05-10 |