| NDC Code | 49580-0808-6 |
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| Package Description | 177 mL in 1 BOTTLE, PLASTIC (49580-0808-6) |
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| Product NDC | 49580-0808 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Mucus Relief Nighttime Cold Flu |
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| Proprietary Name Suffix | Maximum Strengthcold Flu And Sore Throat |
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| Non-Proprietary Name | Acetaminophen, Diphenhydramine Hcl,phenylephrine Hcl |
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| Dosage Form | LIQUID |
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| Usage | ORAL |
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| Start Marketing Date | 20190501 |
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| End Marketing Date | 20241231 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | P & L Development, LLC |
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| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 650; 25; 10 |
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| Strength Unit | mg/20mL; mg/20mL; mg/20mL |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC] |
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