| NDC Code | 50580-369-01 |
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| Package Description | 240 mL in 1 BOTTLE (50580-369-01) |
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| Product NDC | 50580-369 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Tylenol Cold Plus Flu Plus Cough |
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| Proprietary Name Suffix | Night |
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| Non-Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, And Phenylephrine Hydrochloride |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20190617 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M012 |
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| Manufacturer | Johnson & Johnson Consumer Inc. |
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| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 325; 10; 6.25; 5 |
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| Strength Unit | mg/15mL; mg/15mL; mg/15mL; mg/15mL |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Antihistamine [EPC], Histamine Receptor Antagonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
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