mucus relief dm

Generic: dextromethorphan hbr, guaifenesin

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm
Generic Name dextromethorphan hbr, guaifenesin
Labeler walgreen company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-0533
Product ID 0363-0533_8dece8a8-2f8b-4210-b1b6-2710092ab968
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 03630533
Hyphenated Format 0363-0533

Supplemental Identifiers

RxCUI
1147685
UPC
0311917055121
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 (source: ndc)
Generic Name dextromethorphan hbr, guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
  • 400 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (0363-0533-01) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
  • 2 BOTTLE, PLASTIC in 1 CARTON (0363-0533-32) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

0363-0533-01 1 BOTTLE, PLASTIC in 1 CARTON (0363-0533-01) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 0363-0533-32 2 BOTTLE, PLASTIC in 1 CARTON (0363-0533-32) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

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

Linked Drug Pages (1)

Mucus Relief DM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8dece8a8-2f8b-4210-b1b6-2710092ab968", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0311917055121"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["cad5da8c-65a6-44c4-a4c7-38f2c7fe43aa"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0363-0533-01)  / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "0363-0533-01", "marketing_start_date": "20051231"}, {"sample": false, "description": "2 BOTTLE, PLASTIC in 1 CARTON (0363-0533-32)  / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "0363-0533-32", "marketing_start_date": "20051231"}], "brand_name": "Mucus Relief DM", "product_id": "0363-0533_8dece8a8-2f8b-4210-b1b6-2710092ab968", "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": "0363-0533", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "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"}