mucus relief dm maximum strength

Generic: dextromethorphan hbr, guaifenesin

Labeler: cardinal health (leader) 70000
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm maximum strength
Generic Name dextromethorphan hbr, guaifenesin
Labeler cardinal health (leader) 70000
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 400 mg/20mL

Manufacturer
Cardinal Health (Leader) 70000

Identifiers & Regulatory

Product NDC 70000-0565
Product ID 70000-0565_6616d591-2537-4f51-93cf-8a503d660a70
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2020-04-30
Marketing End 2026-08-28

Pharmacologic Class

Established (EPC)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 700000565
Hyphenated Format 70000-0565

Supplemental Identifiers

RxCUI
1020138
UPC
0096295139860
UNII
9D2RTI9KYH 495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name mucus relief dm maximum strength (source: ndc)
Generic Name dextromethorphan hbr, guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/20mL
  • 400 mg/20mL
source: ndc
Packaging
  • 177 mL in 1 BOTTLE, PLASTIC (70000-0565-1)
source: ndc

Packages (1)

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

Ingredients (2)

dextromethorphan hydrobromide (20 mg/20mL) guaifenesin (400 mg/20mL)

Linked Drug Pages (1)

Mucus Relief DM Maximum Strength ndc-match (0.9)

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"}