mucus dm

Generic: dextromethorphan hbr, guaifenesin

Labeler: meijer distribution, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus dm
Generic Name dextromethorphan hbr, guaifenesin
Labeler meijer distribution, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Meijer Distribution, Inc.

Identifiers & Regulatory

Product NDC 79481-5330
Product ID 79481-5330_94fb0ebd-c1ec-48ff-a467-8d212eb3fb9b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2025-03-20

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 794815330
Hyphenated Format 79481-5330

Supplemental Identifiers

RxCUI
1147685
UPC
0708820150676
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 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 (79481-5330-1) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

79481-5330-1 1 BOTTLE, PLASTIC in 1 CARTON (79481-5330-1) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

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

Linked Drug Pages (1)

Mucus DM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "94fb0ebd-c1ec-48ff-a467-8d212eb3fb9b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0708820150676"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["87cf4f25-b0e9-4f8b-bde3-0d0f26e2120e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Meijer Distribution, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (79481-5330-1)  / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "79481-5330-1", "marketing_start_date": "20250320"}], "brand_name": "Mucus DM", "product_id": "79481-5330_94fb0ebd-c1ec-48ff-a467-8d212eb3fb9b", "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": "79481-5330", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "Meijer Distribution, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus 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": "20250320", "listing_expiration_date": "20261231"}