| NDC Code | 68016-686-50 |
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| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (68016-686-50) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
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| Product NDC | 68016-686 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Mucus Relief Pe |
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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 | 20060415 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | Chain Drug Consortium |
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| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 400; 10 |
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| Strength Unit | 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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