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United States · US · US:63868-235_4f7077f9-5790-46dd-88dc-236cd702e250
Mucus Relief DM Max
UNIISPLATC R05DA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerQUALITY CHOICE (Chain Drug Marketing Association)
CountryUS (United States)
ATC codeR05DA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc116386823506177 mL in 1 BOTTLE, PLASTIC (63868-235-06)
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": {
"84b5d83d-aea5-42ed-b20c-96d3b389c8c0": {
"match": "brand_token",
"title": "MUCUS RELIEF DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) TABLET, EXTENDED RELEASE [RITE AID CORPORATION]",
"spl_version": "3",
"published_date": "2026-05-28"
}
},
"productid": "63868-235_4f7077f9-5790-46dd-88dc-236cd702e250",
"productndc": "63868-235",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
"proprietary_name": "Mucus Relief DM Max",
"active_ingred_unit": "mg/20mL; mg/20mL",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Dextromethorphan HBr, Guaifenesin",
"start_marketing_date": "20160331",
"active_numerator_strength": "20; 400"
}Related drugs
Other records sharing ATC code R05DA.
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