qch maximum strength mucus relief dm 628

Generic: dextromethorphan hbr, guaifenesin

Labeler: chain drug marketing association inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name qch maximum strength mucus relief dm 628
Generic Name dextromethorphan hbr, guaifenesin
Labeler chain drug marketing association inc.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

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

Manufacturer
Chain Drug Marketing Association Inc.

Identifiers & Regulatory

Product NDC 83324-026
Product ID 83324-026_a2795bf5-34c6-4de6-b9e5-53a23d18e357
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number part341
Listing Expiration 2026-12-31
Marketing Start 2024-04-26

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 83324026
Hyphenated Format 83324-026

Supplemental Identifiers

RxCUI
1020138
UNII
9D2RTI9KYH 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 qch maximum strength mucus relief dm 628 (source: ndc)
Generic Name dextromethorphan hbr, guaifenesin (source: ndc)
Application Number part341 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/20mL
  • 400 mg/20mL
source: ndc
Packaging
  • 177 mL in 1 BOTTLE (83324-026-06)
source: ndc

Packages (1)

83324-026-06 177 mL in 1 BOTTLE (83324-026-06)

Ingredients (2)

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

Linked Drug Pages (1)

QCH Maximum Strength Mucus Relief DM 628 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a2795bf5-34c6-4de6-b9e5-53a23d18e357", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["a2795bf5-34c6-4de6-b9e5-53a23d18e357"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Chain Drug Marketing Association Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE (83324-026-06)", "package_ndc": "83324-026-06", "marketing_start_date": "20240426"}], "brand_name": "QCH Maximum Strength Mucus Relief DM 628", "product_id": "83324-026_a2795bf5-34c6-4de6-b9e5-53a23d18e357", "dosage_form": "LIQUID", "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": "83324-026", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "Chain Drug Marketing Association Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "QCH Maximum Strength Mucus Relief DM 628", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/20mL"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240426", "listing_expiration_date": "20261231"}