| NDC Code | 50844-548-08 |
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| Package Description | 2 BLISTER PACK in 1 CARTON (50844-548-08) > 12 TABLET, FILM COATED in 1 BLISTER PACK |
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| Product NDC | 50844-548 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Sinus Relief Pe |
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| Proprietary Name Suffix | Maximum Strength |
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| Non-Proprietary Name | 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 | 20030917 |
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| End Marketing Date | 20231011 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | L.N.K. International, Inc. |
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| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 200; 5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
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