| NDC Code | 0031-8752-18 |
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| Package Description | 1 BOTTLE in 1 CARTON (0031-8752-18) / 237 mL in 1 BOTTLE |
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| Product NDC | 0031-8752 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Robitussin Severe Multi-symptom Cough Cold Flu Nighttime |
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| Non-Proprietary Name | Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine Hydrochloride |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20150701 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M0012 |
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| Manufacturer | Haleon US Holdings 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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