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United States · US · US:83324-023_41a95b6d-6e0a-4729-ac06-3963a78a0e51
QCH Adult Tussin DM 542
UNIISPLATC R05DA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerChain Drug Marketing Association Inc.
CountryUS (United States)
ATC codeR05DA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1183324023041 BOTTLE in 1 CARTON (83324-023-04) / 118 mL in 1 BOTTLE
- ndc1183324023081 BOTTLE in 1 CARTON (83324-023-08) / 237 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
9D2RTI9KYH
DEXTROMETHORPHAN HYDROBROMIDE
RxCUI 102490
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "9D2RTI9KYH",
"rxcui": "102490",
"inchikey": "STTADZBLEUMJRG-IKNOHUQMSA-N",
"display_name": "DEXTROMETHORPHAN HYDROBROMIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"a1c5c15e-0f3a-47d3-b9ed-1e0018417514": {
"match": "brand_token",
"title": "QCH MAXIMUM STRENGTH MUCUS RELIEF 617 (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [CHAIN DRUG MARKETING ASSOCIATION INC.]",
"spl_version": "1",
"published_date": "2024-09-09"
}
},
"productid": "83324-023_41a95b6d-6e0a-4729-ac06-3963a78a0e51",
"productndc": "83324-023",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
"proprietary_name": "QCH Adult Tussin DM 542",
"active_ingred_unit": "mg/20mL; mg/20mL",
"application_number": "part341",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Dextromethorphan HBr, Guaifenesin",
"start_marketing_date": "20240508",
"active_numerator_strength": "20; 200"
}Related drugs
Other records sharing ATC code R05DA.
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