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United States · US · US:69168-370_e6dbafa2-0868-44ec-b764-f15b26a97fce
Mucus Relief
UNIISPLATC R05CA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllegiant Health
CountryUS (United States)
ATC codeR05CA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 6
- ndc116916837017300 TABLET in 1 BOTTLE (69168-370-17)
- ndc116916837001100 TABLET in 1 BOTTLE (69168-370-01)
- ndc116916837002150 TABLET in 1 BOTTLE (69168-370-02)
- ndc1169168370301 BOTTLE in 1 CARTON (69168-370-30) / 30 TABLET in 1 BOTTLE
- ndc1169168370411 BOTTLE in 1 CARTON (69168-370-41) / 15 TABLET in 1 BOTTLE
- ndc11691683706060 TABLET in 1 BOTTLE (69168-370-60)
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": "69168-370_e6dbafa2-0868-44ec-b764-f15b26a97fce",
"productndc": "69168-370",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN",
"proprietary_name": "Mucus Relief",
"active_ingred_unit": "mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "GUAIFENESIN",
"start_marketing_date": "20141223",
"active_numerator_strength": "400"
}Related drugs
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