| NDC Code | 55910-529-08 |
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| Package Description | 2 BLISTER PACK in 1 CARTON (55910-529-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK |
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| Product NDC | 55910-529 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Sinus Severe |
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| Proprietary Name Suffix | Daytime |
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| Non-Proprietary Name | Acetaminophen, Guaifenesin, Phenylephrine Hcl |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20050806 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M012 |
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| Manufacturer | DOLGENCORP, 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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