Headache Relief PM 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; Aspirin; Diphenhydramine Citrate.
| Product ID | 55910-674_08c53f73-bd1d-43c8-a1d0-68ff914c3606 |
| NDC | 55910-674 |
| Product Type | Human Otc Drug |
| Proprietary Name | Headache Relief PM |
| Generic Name | Acetaminophen, Aspirin, Diphenhydramine Citrate |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2016-08-31 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Labeler Name | DOLGENCORP, LLC |
| Substance Name | ACETAMINOPHEN; ASPIRIN; DIPHENHYDRAMINE CITRATE |
| Active Ingredient Strength | 250 mg/1; mg/1; mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2016-08-31 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-08-31 |
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 250 mg/1 |
| SPL SET ID: | a2fe05af-7cc2-4981-9557-c5fd589ab2a4 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| Pharm Class PE | |
| PHarm Class EPC | |
| UPC Code | |
| NUI Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0363-9894 | HEADACHE RELIEF PM | ACETAMINOPHEN, ASPIRIN, and DIPHENHYDRAMINE CITRATE |
| 55910-674 | Headache Relief PM | Acetaminophen, Aspirin, Diphenhydramine citrate |
| 63941-373 | Headache Relief PM | Acetaminophen and Diphenhydramine Citrate |
| 63941-674 | Headache Relief PM | Acetaminophen, Aspirin, Diphenhydramine citrate |
| 46122-456 | Pain Relief PM | Acetaminophen, Aspirin, Diphenhydramine citrate |
| 59779-894 | Pain Relief PM | Acetaminophen, Aspirin, Diphenhydramine citrate |