FDA Label Search
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NDC Search Results on Proprietary Name: tylenol
Click on Proprietary Name to view the label.
| Proprietary Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
|---|---|---|---|---|---|
| TYLENOL with Codeine | 50090-0006-2 | A-S Medication Solutions | ANDA085055 | HUMAN PRESCRIPTION DRUG | ANDA |
| TYLENOL 8 HR ARTHRITIS PAIN | 50580-575-01 | Johnson & Johnson Consumer Inc. | ANDA211544 | HUMAN OTC DRUG | ANDA |
| TYLENOL 8 HR ARTHRITIS PAIN | 50580-575-02 | Johnson & Johnson Consumer Inc. | ANDA211544 | HUMAN OTC DRUG | ANDA |
| TYLENOL 8 HR MUSCLE ACHES AND PAIN | 50580-576-02 | Johnson & Johnson Consumer Inc. | ANDA211544 | HUMAN OTC DRUG | ANDA |
| TYLENOL 8 HR ARTHRITIS PAIN | 50580-575-03 | Johnson & Johnson Consumer Inc. | ANDA211544 | HUMAN OTC DRUG | ANDA |
| TYLENOL 8 HR ARTHRITIS PAIN | 50580-575-06 | Johnson & Johnson Consumer Inc. | ANDA211544 | HUMAN OTC DRUG | ANDA |
| TYLENOL 8 HR MUSCLE ACHES AND PAIN | 50580-576-01 | Johnson & Johnson Consumer Inc. | ANDA211544 | HUMAN OTC DRUG | ANDA |
| Motrin Dual Action With Tylenol | 50580-208-08 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
| Motrin Dual Action With Tylenol | 50580-208-02 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
| Motrin Dual Action With Tylenol | 50580-208-12 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
| Motrin Dual Action With Tylenol | 50580-208-16 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
| TYLENOL Cold Plus Flu Severe | 50580-402-02 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL SINUS SEVERE | 29485-8057-2 | Lil' Drug Store Products, Inc. | M012 | HUMAN OTC DRUG | OTC monograph final |
| Tylenol Sinus Severe | 50580-507-04 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol Sinus Severe, TRAVEL BASIX | 66715-7857-2 | Lil Drug Store Products, Inc | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL SINUS SEVERE | 29485-6557-4 | Lil' Drug Store Products, Inc. | M012 | HUMAN OTC DRUG | OTC monograph final |
| Tylenol Sinus Severe | 50580-507-03 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol Cold Plus Head Congestion Severe | 50580-566-25 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| Lil Drug Store Tylenol Sinus Severe | 66715-9757-3 | Lil Drug Store Products, Inc | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| Childrens TYLENOL COLD plus COUGH plus RUNNY NOSE | 50580-245-02 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL Cold Max Day | 50580-515-01 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| Extra Strength TYLENOL Cold Plus Flu Multi-Action Day | 50580-344-01 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL Cold Plus Mucus Severe | 50580-511-01 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| Extra Strength TYLENOL Severe Cough Plus Sore Throat Night | 50580-243-01 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol Cold plus Flu plus Cough Night | 50580-369-01 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL COLD PLUS FLU SEVERE | 29485-8062-3 | Lil' Drug Store Products, Inc. | M012 | HUMAN OTC DRUG | OTC monograph final |
| Tylenol Sinus Severe | 50580-507-01 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol Sinus Severe | 67414-507-04 | Jones Healthcare Group - Packaging Services, Inc | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol Cold plus Flu Severe and Tylenol Cold Max | 50580-241-01 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol Cold Plus Flu Severe Day and Tylenol Cold Plus Flu Plus Cough Night 2-pack | 50580-526-01 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
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