mucus relief d

Generic: guaifenesin, pseudoephedrine hcl

Labeler: meijer distribution inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief d
Generic Name guaifenesin, pseudoephedrine hcl
Labeler meijer distribution inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

guaifenesin 400 mg/1, pseudoephedrine hydrochloride 40 mg/1

Manufacturer
Meijer Distribution Inc

Identifiers & Regulatory

Product NDC 41250-547
Product ID 41250-547_44dcb7ca-3647-4053-a1a9-0dd80c7b8dd0
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2007-01-26

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 41250547
Hyphenated Format 41250-547

Supplemental Identifiers

RxCUI
1090623
UNII
495W7451VQ 6V9V2RYJ8N
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 d (source: ndc)
Generic Name guaifenesin, pseudoephedrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
  • 40 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (41250-547-72) / 9 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (2)

guaifenesin (400 mg/1) pseudoephedrine hydrochloride (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44dcb7ca-3647-4053-a1a9-0dd80c7b8dd0", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ", "6V9V2RYJ8N"], "rxcui": ["1090623"], "spl_set_id": ["383281d7-0d25-4423-ace2-d2985f2c37d0"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (41250-547-72)  / 9 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "41250-547-72", "marketing_start_date": "20070126"}], "brand_name": "Mucus Relief D", "product_id": "41250-547_44dcb7ca-3647-4053-a1a9-0dd80c7b8dd0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "41250-547", "generic_name": "Guaifenesin, Pseudoephedrine HCl", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief D", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20070126", "listing_expiration_date": "20261231"}