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United States · US · US:41250-547_44dcb7ca-3647-4053-a1a9-0dd80c7b8dd0
Mucus Relief D
UNIISPLATC R05CA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMeijer Distribution Inc
CountryUS (United States)
ATC codeR05CA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1141250547723 BLISTER PACK in 1 CARTON (41250-547-72) / 9 TABLET, FILM COATED in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
495W7451VQ
GUAIFENESIN
RxCUI 5032
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "495W7451VQ",
"rxcui": "5032",
"inchikey": "HSRJKNPTNIJEKV-UHFFFAOYSA-N",
"display_name": "GUAIFENESIN",
"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": "41250-547_44dcb7ca-3647-4053-a1a9-0dd80c7b8dd0",
"productndc": "41250-547",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE",
"proprietary_name": "Mucus Relief D",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Guaifenesin, Pseudoephedrine HCl",
"start_marketing_date": "20070126",
"active_numerator_strength": "400; 40"
}Related drugs
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