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United States · US · US:72476-734_5615e45c-82f5-4b61-9f0d-6728e5f8d1df
Mucus Relief DM
Orange BookUNIISPLATC R05DA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCare One (Retail Business Services, LLC.)
CountryUS (United States)
ATC codeR05DA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11724767341414 BLISTER PACK in 1 CARTON (72476-734-14) / 1 TABLET in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
9D2RTI9KYH
DEXTROMETHORPHAN HYDROBROMIDE
RxCUI 102490
Orange Book
A209692
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": "72476-734_5615e45c-82f5-4b61-9f0d-6728e5f8d1df",
"productndc": "72476-734",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "209692",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "30MG;600MG",
"product_no": "001",
"approval_date": "Nov 1, 2018"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "60MG;1.2GM",
"product_no": "002",
"approval_date": "Nov 1, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
"proprietary_name": "Mucus Relief DM",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "ANDA209692",
"marketing_category": "ANDA",
"nonproprietary_name": "Guaifenesin, Dextromethorphan HBr",
"start_marketing_date": "20191129",
"active_numerator_strength": "60; 1200"
}Related drugs
Other records sharing ATC code R05DA.
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