rugby chest congestion relief dm

Generic: dextromethorphan hydrobromide / guaifenesin

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

Drug Facts

Product Profile

Brand Name rugby chest congestion relief dm
Generic Name dextromethorphan hydrobromide / guaifenesin
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 71335-2216
Product ID 71335-2216_c9d9d4bf-2fb0-44d4-b3fa-b16457faf413
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2020-09-01

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 713352216
Hyphenated Format 71335-2216

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 rugby chest congestion relief dm (source: ndc)
Generic Name dextromethorphan hydrobromide / guaifenesin (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 (71335-2216-1)
  • 20 TABLET in 1 BOTTLE (71335-2216-2)
  • 18 TABLET in 1 BOTTLE (71335-2216-3)
  • 60 TABLET in 1 BOTTLE (71335-2216-4)
source: ndc

Packages (4)

71335-2216-1 30 TABLET in 1 BOTTLE (71335-2216-1) 71335-2216-2 20 TABLET in 1 BOTTLE (71335-2216-2) 71335-2216-3 18 TABLET in 1 BOTTLE (71335-2216-3) 71335-2216-4 60 TABLET in 1 BOTTLE (71335-2216-4)

Ingredients (2)

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

Linked Drug Pages (1)

Rugby Chest Congestion Relief DM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c9d9d4bf-2fb0-44d4-b3fa-b16457faf413", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["7b23faa9-40c8-4cea-b9fb-487cce2664af"], "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 (71335-2216-1)", "package_ndc": "71335-2216-1", "marketing_start_date": "20230802"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-2216-2)", "package_ndc": "71335-2216-2", "marketing_start_date": "20240401"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71335-2216-3)", "package_ndc": "71335-2216-3", "marketing_start_date": "20250131"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2216-4)", "package_ndc": "71335-2216-4", "marketing_start_date": "20250131"}], "brand_name": "Rugby Chest Congestion Relief DM", "product_id": "71335-2216_c9d9d4bf-2fb0-44d4-b3fa-b16457faf413", "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": "71335-2216", "generic_name": "Dextromethorphan Hydrobromide / Guaifenesin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Rugby Chest Congestion Relief", "brand_name_suffix": "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": "20200901", "listing_expiration_date": "20261231"}