mucus relief cough and congestion dm

Generic: guaifenesin and dextromethorphan hbr

Labeler: bryant ranch prepack
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief cough and congestion dm
Generic Name guaifenesin and dextromethorphan hbr
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1928
Product ID 71335-1928_8f419f71-24d6-44c8-ba06-e08d7433103e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2016-04-01

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 713351928
Hyphenated Format 71335-1928

Supplemental Identifiers

RxCUI
1147685
UNII
9D2RTI9KYH 495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

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 M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
  • 400 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1928-1)
  • 20 TABLET in 1 BOTTLE (71335-1928-2)
  • 18 TABLET in 1 BOTTLE (71335-1928-3)
source: ndc

Packages (3)

71335-1928-1 30 TABLET in 1 BOTTLE (71335-1928-1) 71335-1928-2 20 TABLET in 1 BOTTLE (71335-1928-2) 71335-1928-3 18 TABLET in 1 BOTTLE (71335-1928-3)

Ingredients (2)

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

Linked Drug Pages (1)

Mucus Relief Cough and Congestion DM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8f419f71-24d6-44c8-ba06-e08d7433103e", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["8c25285e-e2cd-4e10-af63-5dce8098b615"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1928-1)", "package_ndc": "71335-1928-1", "marketing_start_date": "20210811"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-1928-2)", "package_ndc": "71335-1928-2", "marketing_start_date": "20210811"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71335-1928-3)", "package_ndc": "71335-1928-3", "marketing_start_date": "20210811"}], "brand_name": "Mucus Relief Cough and Congestion DM", "product_id": "71335-1928_8f419f71-24d6-44c8-ba06-e08d7433103e", "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": "71335-1928", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "Bryant Ranch Prepack", "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": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160401", "listing_expiration_date": "20261231"}