qch adult tussin 541

Generic: guaifenesin

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

Drug Facts

Product Profile

Brand Name qch adult tussin 541
Generic Name guaifenesin
Labeler chain drug marketing association inc.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

guaifenesin 200 mg/10mL

Manufacturer
Chain Drug Marketing Association Inc.

Identifiers & Regulatory

Product NDC 83324-024
Product ID 83324-024_b487f4af-ad0c-4f18-9a6b-7fd386b3f46c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number part341
Listing Expiration 2026-12-31
Marketing Start 2024-05-02

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 83324024
Hyphenated Format 83324-024

Supplemental Identifiers

RxCUI
310604
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 qch adult tussin 541 (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number part341 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/10mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (83324-024-04) / 118 mL in 1 BOTTLE
source: ndc

Packages (1)

83324-024-04 1 BOTTLE in 1 CARTON (83324-024-04) / 118 mL in 1 BOTTLE

Ingredients (1)

guaifenesin (200 mg/10mL)

Linked Drug Pages (1)

QCH Adult Tussin 541 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b487f4af-ad0c-4f18-9a6b-7fd386b3f46c", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310604"], "spl_set_id": ["b487f4af-ad0c-4f18-9a6b-7fd386b3f46c"], "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": "1 BOTTLE in 1 CARTON (83324-024-04)  / 118 mL in 1 BOTTLE", "package_ndc": "83324-024-04", "marketing_start_date": "20240502"}], "brand_name": "QCH Adult Tussin 541", "product_id": "83324-024_b487f4af-ad0c-4f18-9a6b-7fd386b3f46c", "dosage_form": "LIQUID", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "83324-024", "generic_name": "Guaifenesin", "labeler_name": "Chain Drug Marketing Association Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "QCH Adult Tussin 541", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "200 mg/10mL"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240502", "listing_expiration_date": "20261231"}