mucus relief dm max

Generic: dextromethorphan hbr, guaifenesin

Labeler: dolgencorp, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm max
Generic Name dextromethorphan hbr, guaifenesin
Labeler dolgencorp, llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

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

Manufacturer
DOLGENCORP, LLC

Identifiers & Regulatory

Product NDC 55910-146
Product ID 55910-146_31cc6e32-7897-49f0-a18f-b105a8a90acf
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-10-07

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 55910146
Hyphenated Format 55910-146

Supplemental Identifiers

RxCUI
1020138
UPC
0350844657954
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 max (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
  • 266 mL in 1 BOTTLE, PLASTIC (55910-146-95)
source: ndc

Packages (1)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31cc6e32-7897-49f0-a18f-b105a8a90acf", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0350844657954"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["5be4e730-3cd6-414e-a23b-f6cad8088750"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["DOLGENCORP, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "266 mL in 1 BOTTLE, PLASTIC (55910-146-95)", "package_ndc": "55910-146-95", "marketing_start_date": "20241007"}], "brand_name": "Mucus Relief DM Max", "product_id": "55910-146_31cc6e32-7897-49f0-a18f-b105a8a90acf", "dosage_form": "SOLUTION", "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": "55910-146", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "DOLGENCORP, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM Max", "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": "20241007", "listing_expiration_date": "20261231"}