mucus relief cough and congestion dm
Generic: guaifenesin and dextromethorphan hbr
Labeler: richmond pharmaceuticals, incDrug Facts
Product Profile
Brand Name
mucus relief cough and congestion dm
Generic Name
guaifenesin and dextromethorphan hbr
Labeler
richmond pharmaceuticals, inc
Dosage Form
TABLET
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/1, guaifenesin 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
54738-985
Product ID
54738-985_5cc409a8-23e1-738f-e053-2a91aa0ac0d5
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH FINAL
Application Number
part341
Listing Expiration
2026-12-31
Marketing Start
2016-04-01
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
54738985
Hyphenated Format
54738-985
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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 cough and congestion dm (source: ndc)
Generic Name
guaifenesin and dextromethorphan hbr (source: ndc)
Application Number
part341 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
- 400 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (54738-985-30)
- 60 TABLET in 1 BOTTLE (54738-985-60)
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5cc409a8-23e1-738f-e053-2a91aa0ac0d5", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0054738985306"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["59b00858-e5c9-420a-bc7e-46953722cde6"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Richmond Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (54738-985-30)", "package_ndc": "54738-985-30", "marketing_start_date": "20160401"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (54738-985-60)", "package_ndc": "54738-985-60", "marketing_start_date": "20160401"}], "brand_name": "Mucus Relief Cough and Congestion DM", "product_id": "54738-985_5cc409a8-23e1-738f-e053-2a91aa0ac0d5", "dosage_form": "TABLET", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "54738-985", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "Richmond Pharmaceuticals, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Cough and Congestion DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/1"}, {"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20160401", "listing_expiration_date": "20261231"}