Package 70000-0565-1

Brand: mucus relief dm maximum strength

Generic: dextromethorphan hbr, guaifenesin
NDC Package

Package Facts

Identity

Package NDC 70000-0565-1
Digits Only 7000005651
Product NDC 70000-0565
Description

177 mL in 1 BOTTLE, PLASTIC (70000-0565-1)

Marketing

Marketing Status
Discontinued 2026-08-28
Brand mucus relief dm 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": "6616d591-2537-4f51-93cf-8a503d660a70", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0096295139860"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["c4971d15-c768-4370-b7b3-f0b4848e1758"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Cardinal Health (Leader) 70000"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, PLASTIC (70000-0565-1)", "package_ndc": "70000-0565-1", "marketing_end_date": "20260828", "marketing_start_date": "20200430"}], "brand_name": "Mucus Relief DM Maximum Strength", "product_id": "70000-0565_6616d591-2537-4f51-93cf-8a503d660a70", "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": "70000-0565", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "Cardinal Health (Leader) 70000", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "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_end_date": "20260828", "marketing_start_date": "20200430"}