mucus relief dm maximum strength

Generic: dextromethorphan hydrobromide, guaifenesin

Labeler: walgreens
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm maximum strength
Generic Name dextromethorphan hydrobromide, guaifenesin
Labeler walgreens
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

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

Manufacturer
Walgreens

Identifiers & Regulatory

Product NDC 0363-0505
Product ID 0363-0505_0172aeab-6e08-4e57-ac98-b7f10eb8a6da
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2017-08-31

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 03630505
Hyphenated Format 0363-0505

Supplemental Identifiers

RxCUI
1020138
UPC
0311917159485
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 hydrobromide, 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 (0363-0505-06)
source: ndc

Packages (1)

0363-0505-06 177 mL in 1 BOTTLE (0363-0505-06)

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": "0172aeab-6e08-4e57-ac98-b7f10eb8a6da", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0311917159485"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["397e83c6-d81a-4cfd-bfb9-e7ba7659e090"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE (0363-0505-06)", "package_ndc": "0363-0505-06", "marketing_start_date": "20170831"}], "brand_name": "Mucus Relief DM Maximum Strength", "product_id": "0363-0505_0172aeab-6e08-4e57-ac98-b7f10eb8a6da", "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": "0363-0505", "generic_name": "dextromethorphan hydrobromide, guaifenesin", "labeler_name": "Walgreens", "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_start_date": "20170831", "listing_expiration_date": "20261231"}