| NDC Code | 50580-257-08 |
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| Package Description | 240 mL in 1 BOTTLE, PLASTIC (50580-257-08) |
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| Product NDC | 50580-257 |
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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 | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20060701 |
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| End Marketing Date | 20161231 |
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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/15mL; mg/15mL; mg/15mL |
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