| NDC Code | 68210-4164-1 |
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| Package Description | 1 BOTTLE in 1 CARTON (68210-4164-1) / 12 TABLET, FILM COATED in 1 BOTTLE |
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| Product NDC | 68210-4164 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Non-drowsy Daytime Severe Sinus Congestion And Pain |
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| Non-Proprietary Name | Acetaminophen, Guaifenesin And Phenylephrine Hcl |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20210623 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M012 |
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| Manufacturer | Spirit Pharmaceuticals LLC |
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| Substance Name | ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 325; 200; 5 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-1 Adrenergic Agonist [EPC] |
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