mucus relief

Generic: guaifenesin 400 mg

Labeler: twin med llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief
Generic Name guaifenesin 400 mg
Labeler twin med llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 400 mg/1

Manufacturer
TWIN MED LLC

Identifiers & Regulatory

Product NDC 55681-311
Product ID 55681-311_3906e938-65b3-d3e3-e063-6294a90a3020
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2022-07-01

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 55681311
Hyphenated Format 55681-311

Supplemental Identifiers

RxCUI
359601
UPC
0816516015496
UNII
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 (source: ndc)
Generic Name guaifenesin 400 mg (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 300 TABLET in 1 BOTTLE (55681-311-03)
source: ndc

Packages (1)

Ingredients (1)

guaifenesin (400 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3906e938-65b3-d3e3-e063-6294a90a3020", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0816516015496"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["e31bd69f-97ab-9d99-e053-2995a90a580e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["TWIN MED LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (55681-311-03)", "package_ndc": "55681-311-03", "marketing_start_date": "20220701"}], "brand_name": "Mucus Relief", "product_id": "55681-311_3906e938-65b3-d3e3-e063-6294a90a3020", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "55681-311", "generic_name": "Guaifenesin 400 mg", "labeler_name": "TWIN MED LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220701", "listing_expiration_date": "20261231"}