| NDC Code | 50580-406-24 |
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| Package Description | 2 BLISTER PACK in 1 CARTON (50580-406-24) > 12 TABLET, FILM COATED in 1 BLISTER PACK |
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| Product NDC | 50580-406 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Tylenol Cold Multi-symptom Daytime |
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| Non-Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, And Phenylephrine Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20120701 |
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| End Marketing Date | 20170331 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
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| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 325; 10; 5 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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