mucus relief dm immediate release

Generic: mucus relief dm

Labeler: good sense
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm immediate release
Generic Name mucus relief dm
Labeler good sense
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
Good Sense

Identifiers & Regulatory

Product NDC 50804-432
Product ID 50804-432_54b3c3cc-9664-417d-8ffe-391708e4c58a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2022-05-18

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 50804432
Hyphenated Format 50804-432

Supplemental Identifiers

RxCUI
1147685
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 immediate release (source: ndc)
Generic Name mucus relief dm (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 in 1 CARTON (50804-432-30) / 30 TABLET in 1 BOTTLE
source: ndc

Packages (1)

50804-432-30 1 BOTTLE in 1 CARTON (50804-432-30) / 30 TABLET in 1 BOTTLE

Ingredients (2)

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

Linked Drug Pages (1)

Mucus Relief DM Immediate Release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "54b3c3cc-9664-417d-8ffe-391708e4c58a", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["26a199bf-57e5-4f36-b40c-83a1187e4870"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Good Sense"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50804-432-30)  / 30 TABLET in 1 BOTTLE", "package_ndc": "50804-432-30", "marketing_start_date": "20220518"}], "brand_name": "Mucus Relief DM Immediate Release", "product_id": "50804-432_54b3c3cc-9664-417d-8ffe-391708e4c58a", "dosage_form": "TABLET", "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": "50804-432", "generic_name": "Mucus Relief DM", "labeler_name": "Good Sense", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "brand_name_suffix": "Immediate Release", "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": "20220518", "listing_expiration_date": "20261231"}