| NDC Code | 50066-917-18 |
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| Package Description | 1 BOTTLE in 1 CARTON (50066-917-18) > 177 mL in 1 BOTTLE |
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| Product NDC | 50066-917 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Tukol Max Action Severe Congestion And Cough |
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| Non-Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin And Phenylephrine Hydrochloride |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20171115 |
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| End Marketing Date | 20220622 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | Genomma Lab USA Inc |
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| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 20; 400; 10 |
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| Strength Unit | mg/20mL; mg/20mL; mg/20mL |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
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