| NDC Code | 0031-2249-04 |
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| Package Description | 1 BOTTLE in 1 CARTON (0031-2249-04) > 118 mL in 1 BOTTLE |
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| Product NDC | 0031-2249 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Childrens Dimetapp Multi-symptom Cold And Flu |
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| Non-Proprietary Name | Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine Hydrochloride |
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| Dosage Form | LIQUID |
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| Usage | ORAL |
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| Start Marketing Date | 20200101 |
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| End Marketing Date | 20220930 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
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| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 320; 12.5; 5 |
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| Strength Unit | mg/10mL; mg/10mL; mg/10mL |
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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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