Mucus Relief DM Maximum Strength

Generic: Dextromethorphan HBr, Guaifenesin

Labeler: Rite Aid Corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive

Drug Facts

Product Profile

Brand Name Mucus Relief DM Maximum Strength
Generic Name Dextromethorphan HBr, Guaifenesin
Labeler Rite Aid Corporation
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

DEXTROMETHORPHAN HYDROBROMIDE 20 mg/20mL, GUAIFENESIN 400 mg/20mL

Identifiers & Regulatory

Product NDC 11822-7224
Product ID 11822-7224_07bca099-4c6d-478d-bd8a-5977907ba435
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2021-11-26
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 118227224
Hyphenated Format 11822-7224

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
  • 117 mL in 1 BOTTLE (11822-7224-6)
source: ndc

Packages (1)

11822-7224-6 117 mL in 1 BOTTLE (11822-7224-6)

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": "07bca099-4c6d-478d-bd8a-5977907ba435", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0011822372244"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["552c942a-ae19-4e48-8bb7-198cd4e24a12"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "117 mL in 1 BOTTLE (11822-7224-6)", "package_ndc": "11822-7224-6", "marketing_end_date": "20260228", "marketing_start_date": "20211126"}], "brand_name": "Mucus Relief DM Maximum Strength", "product_id": "11822-7224_07bca099-4c6d-478d-bd8a-5977907ba435", "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": "11822-7224", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "Rite Aid Corporation", "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": "20260228", "marketing_start_date": "20211126"}