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 Extra Strength | 50580-590-05 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL Extra Strength | 50580-590-06 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL SINUS PLUS HEADACHE DAY | 50580-598-01 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL SINUS PLUS HEADACHE DAY | 50580-598-02 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
| Infants TYLENOL | 50580-599-01 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Infants TYLENOL | 50580-599-02 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Infants TYLENOL | 50580-599-03 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL Regular Strength | 50580-600-01 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL Regular Strength | 50580-600-02 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL Regular Strength | 50580-600-03 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol PM Extra Strength | 50580-608-01 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol PM Extra Strength | 50580-608-02 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol PM Extra Strength | 50580-608-03 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol PM Extra Strength | 50580-608-04 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol PM Extra Strength | 50580-608-05 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol PM Extra Strength | 50580-608-06 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol PM Extra Strength | 50580-608-07 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol PM Extra Strength | 50580-608-08 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Childrens TYLENOL | 50580-612-01 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Childrens TYLENOL | 50580-612-02 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Childrens TYLENOL | 50580-614-01 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL Extra Strength | 50580-692-01 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL Extra Strength | 50580-692-02 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| TYLENOL Extra Strength | 50580-692-03 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
| Tylenol 8 HR Arthritis Pain | 50580-783-10 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
| Tylenol 8 HR Arthritis Pain | 50580-783-24 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
| Tylenol 8 HR Arthritis Pain | 50580-783-25 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
| Tylenol 8 HR Arthritis Pain | 50580-783-29 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
| Tylenol 8 HR Arthritis Pain | 50580-783-30 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
| Tylenol 8 HR Arthritis Pain | 50580-783-31 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
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