Package 36800-605-06

Brand: mucus relief dm max maximum strength

Generic: dextromethorphan hbr, guaifenesin
NDC Package

Package Facts

Identity

Package NDC 36800-605-06
Digits Only 3680060506
Product NDC 36800-605
Description

177 mL in 1 BOTTLE, PLASTIC (36800-605-06)

Marketing

Marketing Status
Marketed Since 2016-04-30
Brand mucus relief dm max maximum strength
Generic dextromethorphan hbr, guaifenesin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b0015f7d-7eb0-4a76-a83d-85576051d9c7", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0036800386174"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["aa1eb90c-e565-455f-8978-6f2f9e00a814"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["TOP CARE (Topco Associates LLC)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, PLASTIC (36800-605-06)", "package_ndc": "36800-605-06", "marketing_start_date": "20160430"}], "brand_name": "Mucus Relief DM Max Maximum Strength", "product_id": "36800-605_b0015f7d-7eb0-4a76-a83d-85576051d9c7", "dosage_form": "LIQUID", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "36800-605", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "TOP CARE (Topco Associates LLC)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM Max", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160430", "listing_expiration_date": "20261231"}