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United States · US · US:67618-120_8319c8b6-8d3f-416d-a864-39cb879df2da
Senokot
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAtlantis Consumer Healthcare, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc11676181200636 TABLET, FILM COATED in 1 BOTTLE (67618-120-06)
- ndc1167618120121 BLISTER PACK in 1 CARTON (67618-120-12) / 12 TABLET, FILM COATED in 1 BLISTER PACK
- ndc1167618120722 CARTON in 1 PACKAGE (67618-120-72) / 1 BOTTLE in 1 CARTON / 36 TABLET, FILM COATED in 1 BOTTLE
- ndc11676181207372 TABLET, FILM COATED in 1 BOTTLE (67618-120-73)
Annotations
UNII (FDA Substance ID)
3FYP5M0IJX
SENNOSIDES
RxCUI 36387
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "3FYP5M0IJX",
"rxcui": "36387",
"inchikey": null,
"display_name": "SENNOSIDES",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c18dd7fa-993b-440b-8cdd-f1551abb99ca": {
"match": "brand_token",
"title": "SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [ATLANTIS CONSUMER HEALTHCARE, INC.]",
"spl_version": "12",
"published_date": "2025-12-31"
}
},
"productid": "67618-120_8319c8b6-8d3f-416d-a864-39cb879df2da",
"productndc": "67618-120",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "SENNOSIDES",
"proprietary_name": "Senokot",
"active_ingred_unit": "mg/1",
"application_number": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "standardized senna concentrate",
"start_marketing_date": "19880901",
"active_numerator_strength": "17.2"
}Access this data programmatically
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