| NDC Code | 49580-0335-9 |
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| Package Description | 237 mL in 1 BOTTLE, PLASTIC (49580-0335-9) |
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| Product NDC | 49580-0335 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Mucus Relief |
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| Proprietary Name Suffix | Cold And Sinus Maximum Strength |
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| Non-Proprietary Name | Acetaminophen, Guaifenesin, Phenylephrine Hcl |
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| Dosage Form | LIQUID |
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| Usage | ORAL |
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| Start Marketing Date | 20150228 |
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| End Marketing Date | 20241231 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | P & L Development, LLC |
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| Substance Name | ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 650; 400; 10 |
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| Strength Unit | mg/20mL; mg/20mL; mg/20mL |
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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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