TYLENOL PM Extra Strength is a Oral Solution in the Human Otc Drug category. It is labeled and distributed by Johnson & Johnson Consumer Inc., Mcneil Consumer Healthcare Division. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.
| Product ID | 50580-833_814e1ca7-04b5-48a6-8e2b-53250affb22b |
| NDC | 50580-833 |
| Product Type | Human Otc Drug |
| Proprietary Name | TYLENOL PM Extra Strength |
| Generic Name | Acetaminophen And Diphenhydramine Hydrochloride |
| Dosage Form | Solution |
| Route of Administration | ORAL |
| Marketing Start Date | 2018-06-25 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Labeler Name | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Active Ingredient Strength | 1000 mg/30mL; mg/30mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2018-06-25 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2018-06-25 |
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 1000 mg/30mL |
| SPL SET ID: | 44e8a92a-748b-4dc3-ae8d-176a350ac83d |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 67414-608 | Tylenol PM Extra Strength | Tylenol PM Extra Strength |
| 0536-1003 | ACETA-GESIC | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE |
| 30142-193 | Acetaminophen and Diphenhydramine hydrochloride | Acetaminophen and Diphenhydramine hydrochloride |
| 49035-026 | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | ACETAMINOPHEN and DIPHENHYDRAMINE HYDROCHLORIDE |
| 52204-124 | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE |
| 37012-771 | Acetaminophen PM | Acetaminophen and Diphenhydramine Hydrochloride |
| 41163-515 | Acetaminophen PM | Acetaminophen and Diphenhydramine Hydrochloride |
| 57344-095 | Acetaminophen PM | Acetaminophen and DIPHENHYDRAMINE HYDROCHLORIDE |
| 30142-755 | Extra Strength Acetaminophen PM | Acetaminophen and Diphenhydramine Hydrochloride |
| 21130-095 | Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
| 36800-095 | Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
| 36800-771 | Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
| 37808-795 | Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
| 41250-195 | pain relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
| 49738-783 | Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
| 50804-825 | Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
| 15127-033 | Pain Reliever PM | Acetaminophen and Diphenhydramine Hydrochloride |
| 0031-8770 | Robitussin Honey Severe Cough, Flu Plus Sore Throat Nighttime | acetaminophen and diphenhydramine hydrochloride |
| 50405-007 | SohMed Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
| 49483-356 | TIME-GESIC | ACETAMINOPHEN AND 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 |
| 41167-0040 | Unisom PM Pain Nighttime Sleep Aid and Pain Reliever | Acetaminophen and Diphenhydramine Hydrochloride |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TYLENOL PM 74143985 1777613 Live/Registered |
JOHNSON & JOHNSON 1991-03-04 |