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United States · US · US:10956-845_425102a9-bdd6-4b48-8758-503659b1b7b9
Refenesen Mucus Relief
UNIISPLATC R05CA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerReese Pharmaceutical Co
CountryUS (United States)
ATC codeR05CA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1110956845301 BOTTLE, PLASTIC in 1 CARTON (10956-845-30) / 30 TABLET 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": {
"861dffb7-8bf4-4f03-bcc2-ed8a35bc341d": {
"match": "brand_token",
"title": "REFENESEN MUCUS RELIEF (GUAIFENESIN) TABLET [REESE PHARMACEUTICAL CO]",
"spl_version": "4",
"published_date": "2024-12-20"
}
},
"productid": "10956-845_425102a9-bdd6-4b48-8758-503659b1b7b9",
"productndc": "10956-845",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN",
"proprietary_name": "Refenesen Mucus Relief",
"active_ingred_unit": "mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Guaifenesin",
"start_marketing_date": "20210415",
"active_numerator_strength": "400"
}Related drugs
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