Tylenol PM is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Jc World Bell Wholesale Co., Inc.. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.
| Product ID | 50269-608_746da587-727b-29ef-e053-2991aa0a58ba | 
| NDC | 50269-608 | 
| Product Type | Human Otc Drug | 
| Proprietary Name | Tylenol PM | 
| Generic Name | Acetaminophen, Diphenhydramine Hydrochloride | 
| Dosage Form | Tablet | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2018-08-16 | 
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL | 
| Application Number | part343 | 
| Labeler Name | JC World Bell Wholesale Co., Inc. | 
| 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 | 2018-08-16 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | OTC monograph not final | 
| Application Number | part343 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-08-16 | 
| Ingredient | Strength | 
|---|---|
| ACETAMINOPHEN | 500 mg/1 | 
| SPL SET ID: | 83df6b68-8bb5-410b-bb97-0a5eecf424f2 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 50269-608 | Tylenol PM | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE | 
| 50580-608 | Tylenol PM | acetaminophen and diphenhydramine hydrochloride | 
| 50580-833 | TYLENOL PM | Acetaminophen and Diphenhydramine Hydrochloride | 
| 52904-945 | Tylenol PM | acetaminophen and diphenhydramine hydrochloride | 
| 67414-608 | Tylenol PM | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE | 
| 67751-168 | Tylenol PM | Tylenol PM | 
| 73097-013 | Tylenol PM | Tylenol PM | 
| 0536-1173 | Acetaminophen, Diphenhydramine Hydrochloride | Acetaminophen, Diphenhydramine Hydrochloride | 
| 0904-6731 | Acetaminophen, Diphenhydramine Hydrochloride | Acetaminophen, Diphenhydramine Hydrochloride | 
| 58602-216 | Aurophen Pain Away plus Sleep aid | acetaminophen, diphenhydramine hydrochloride | 
| 58602-217 | Aurophen Pain Away plus Sleep aid | acetaminophen, diphenhydramine hydrochloride | 
| 62011-0024 | Extra Strength Acetaminophen PM | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE | 
| 0904-7651 | Extra Strength Mapap PM | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE | 
| 59726-360 | Extra Strength Pain Relief PM | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE | 
| 0363-8590 | NightTime Pain Reliever PM | acetaminophen, diphenhydramine hydrochloride | 
| 10202-946 | Pain Away plus Sleep aid | acetaminophen, diphenhydramine hydrochloride | 
| 46122-358 | Pain Plus Sleep | acetaminophen, diphenhydramine hydrochloride | 
| 55910-996 | Pain Relief plus Sleep Aid | acetaminophen, diphenhydramine hydrochloride | 
| 53943-028 | Pain Relief PM | acetaminophen, diphenhydramine hydrochloride | 
| 55319-998 | Pain Relief PM | acetaminophen, diphenhydramine hydrochloride | 
| 59779-905 | Pain Relief PM | acetaminophen, diphenhydramine hydrochloride | 
| 54257-278 | Pain Reliever PM | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE | 
Mark Image Registration | Serial  | Company  Trademark Application Date  | 
|---|---|
![]() TYLENOL PM  74143985  1777613 Live/Registered  | 
        JOHNSON & JOHNSON  1991-03-04  |