mucus relief dm cough maximum strength

Generic: dextromethorphan hbr and guaifenesin

Labeler: cardinal health 110, llc. dba leader
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm cough maximum strength
Generic Name dextromethorphan hbr and guaifenesin
Labeler cardinal health 110, llc. dba leader
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 20 mg/1, guaifenesin 400 mg/1

Manufacturer
Cardinal Health 110, LLC. DBA Leader

Identifiers & Regulatory

Product NDC 70000-0278
Product ID 70000-0278_63b596e2-a30f-4587-86ed-f0fc724b2f7e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2005-12-31

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 700000278
Hyphenated Format 70000-0278

Supplemental Identifiers

RxCUI
1147685
UPC
0096295131802
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 cough maximum strength (source: ndc)
Generic Name dextromethorphan hbr and guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
  • 400 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (70000-0278-1) / 12 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

70000-0278-1 2 BLISTER PACK in 1 CARTON (70000-0278-1) / 12 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (2)

dextromethorphan hydrobromide (20 mg/1) guaifenesin (400 mg/1)

Linked Drug Pages (1)

Mucus Relief DM Cough Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "63b596e2-a30f-4587-86ed-f0fc724b2f7e", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0096295131802"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["6304a581-9238-4539-b157-293fc05c173e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Cardinal Health 110, LLC. DBA Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (70000-0278-1)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "70000-0278-1", "marketing_start_date": "20051231"}], "brand_name": "Mucus Relief DM Cough Maximum Strength", "product_id": "70000-0278_63b596e2-a30f-4587-86ed-f0fc724b2f7e", "dosage_form": "TABLET, FILM COATED", "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": "70000-0278", "generic_name": "Dextromethorphan HBr and Guaifenesin", "labeler_name": "Cardinal Health 110, LLC. DBA Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM Cough", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/1"}, {"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20051231", "listing_expiration_date": "20261231"}