qch adult tussin dm 542
Generic: dextromethorphan hbr, guaifenesin
Labeler: chain drug marketing association inc.Drug Facts
Product Profile
Brand Name
qch adult tussin dm 542
Generic Name
dextromethorphan hbr, guaifenesin
Labeler
chain drug marketing association inc.
Dosage Form
LIQUID
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 200 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
83324-023
Product ID
83324-023_41a95b6d-6e0a-4729-ac06-3963a78a0e51
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
part341
Listing Expiration
2026-12-31
Marketing Start
2024-05-08
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83324023
Hyphenated Format
83324-023
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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 dm 542 (source: ndc)
Generic Name
dextromethorphan hbr, guaifenesin (source: ndc)
Application Number
part341 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/20mL
- 200 mg/20mL
Packaging
- 1 BOTTLE in 1 CARTON (83324-023-04) / 118 mL in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (83324-023-08) / 237 mL in 1 BOTTLE
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41a95b6d-6e0a-4729-ac06-3963a78a0e51", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1790650"], "spl_set_id": ["17caffa4-a264-7f3e-e063-6394a90ac419"], "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 (83324-023-04) / 118 mL in 1 BOTTLE", "package_ndc": "83324-023-04", "marketing_start_date": "20240508"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (83324-023-08) / 237 mL in 1 BOTTLE", "package_ndc": "83324-023-08", "marketing_start_date": "20240508"}], "brand_name": "QCH Adult Tussin DM 542", "product_id": "83324-023_41a95b6d-6e0a-4729-ac06-3963a78a0e51", "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": "83324-023", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "Chain Drug Marketing Association Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "QCH Adult Tussin DM 542", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/20mL"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240508", "listing_expiration_date": "20261231"}