| NDC Code | 0067-8124-06 |
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| Package Description | 6 POWDER in 1 CARTON (0067-8124-06) |
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| Product NDC | 0067-8124 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Theraflu Nighttime Multi-symptom Severe Cold Powder |
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| Non-Proprietary Name | Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine Hydrochloride |
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| Dosage Form | POWDER |
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| Usage | ORAL |
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| Start Marketing Date | 20150715 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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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 | 500; 25; 10 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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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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