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United States · US · US:70000-0141_59fa21ab-5e68-467b-90bf-2c8a3e96709b
Mucus Relief PE Sinus Congestion
UNIISPLATC R05CA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCardinal Health 110, LLC. DBA Leader
CountryUS (United States)
ATC codeR05CA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1170000014111 BOTTLE, PLASTIC in 1 CARTON (70000-0141-1) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
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": "70000-0141_59fa21ab-5e68-467b-90bf-2c8a3e96709b",
"productndc": "70000-0141",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE",
"proprietary_name": "Mucus Relief PE Sinus Congestion",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Guaifenesin, Phenylephrine HCl",
"start_marketing_date": "20060415",
"active_numerator_strength": "400; 10"
}Related drugs
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