Mucus Relief

Generic: Guaifenesin

Labeler: Chain Drug Consortium
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive

Drug Facts

Product Profile

Brand Name Mucus Relief
Generic Name Guaifenesin
Labeler Chain Drug Consortium
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

GUAIFENESIN 400 mg/1

Identifiers & Regulatory

Product NDC 68016-545
Product ID 68016-545_3bb70627-72dc-4e52-95a4-d23661a5ffb5
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2023-01-09
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68016545
Hyphenated Format 68016-545

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 (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (68016-545-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

68016-545-50 1 BOTTLE, PLASTIC in 1 CARTON (68016-545-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Ingredients (1)

GUAIFENESIN (400 mg/1)

Linked Drug Pages (1)

Mucus Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3bb70627-72dc-4e52-95a4-d23661a5ffb5", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0840986037696"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["b2e88323-5af9-4ec8-bb98-4da0a774e54e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Chain Drug Consortium"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-545-50)  / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-545-50", "marketing_end_date": "20260228", "marketing_start_date": "20230109"}], "brand_name": "Mucus Relief", "product_id": "68016-545_3bb70627-72dc-4e52-95a4-d23661a5ffb5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "68016-545", "generic_name": "Guaifenesin", "labeler_name": "Chain Drug Consortium", "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_end_date": "20260228", "marketing_start_date": "20230109"}