Pain Relief Acetaminophen PM is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rite Aid Corporation. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.
| Product ID | 11822-0556_57ca8a6e-d692-4d3c-9f7e-163a97023fbc |
| NDC | 11822-0556 |
| Product Type | Human Otc Drug |
| Proprietary Name | Pain Relief Acetaminophen PM |
| Generic Name | Acetaminophen And Diphenhydramine Hcl |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2007-12-17 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Labeler Name | Rite Aid Corporation |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Active Ingredient Strength | 500 mg/1; mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2007-12-17 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2007-12-17 |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2007-12-17 |
| Marketing End Date | 2019-05-17 |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2007-12-17 |
| Marketing End Date | 2020-06-15 |
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 500 mg/1 |
| SPL SET ID: | f77f0120-4042-4b11-ba9c-cd35e1cd0bee |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 11822-0556 | Pain Relief Acetaminophen PM | Acetaminophen and Diphenhydramine HCl |
| 11822-2350 | Pain Relief Acetaminophen PM | Acetaminophen and Diphenhydramine HCl |
| 0536-3479 | Acetaminophen and Diphenhydramine HCl | Acetaminophen and Diphenhydramine HCl |
| 49035-235 | Acetaminophen PM | Acetaminophen and Diphenhydramine HCl |
| 55319-235 | Acetaminophen PM | Acetaminophen and Diphenhydramine HCl |
| 55319-556 | Acetaminophen PM | Acetaminophen and Diphenhydramine HCl |
| 58602-743 | Aurophen PM Extra Strength | Acetaminophen and Diphenhydramine HCl |
| 37205-759 | Extra Strength Pain Reliever PM | Acetaminophen and Diphenhydramine HCl |
| 49738-999 | KMart - Pain Relief PM | Acetaminophen and Diphenhydramine HCl |
| 21130-556 | Pain Relief PM | Acetaminophen and Diphenhydramine HCl |
| 49738-655 | Pain Relief PM | Acetaminophen and Diphenhydramine HCl |
| 55910-655 | Pain Relief PM | Acetaminophen and Diphenhydramine HCl |
| 15127-325 | Pain Reliever PM | Acetaminophen and Diphenhydramine HCl |
| 0135-0608 | PANADOL | acetaminophen and diphenhydramine HCl |
| 0135-7021 | PANADOL | acetaminophen and diphenhydramine HCl |
| 41250-556 | Rapid Release Pain Relief PM | Acetaminophen and Diphenhydramine HCl |
| 0363-0235 | Wal-Nadol PM | Acetaminophen and Diphenhydramine HCl |