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United States · US · US:69842-220_28513391-e716-29a1-e063-6394a90a0340
SENNOSIDES
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCVS Pharmacy, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc116984222008500 TABLET, FILM COATED in 1 BOTTLE (69842-220-08)
- ndc116984222025250 TABLET, FILM COATED in 1 BOTTLE (69842-220-25)
- ndc1169842220501 BOTTLE in 1 CARTON (69842-220-50) / 50 TABLET, FILM COATED in 1 BOTTLE
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": {
"40385b89-a855-4ca2-992a-df5eb677be15": {
"match": "brand_token",
"title": "SENNOSIDES AND DOCUSATE SODIUM TABLET [CARDINAL HEALTH 107, LLC]",
"spl_version": "7",
"published_date": "2026-05-25"
}
},
"productid": "69842-220_28513391-e716-29a1-e063-6394a90a0340",
"productndc": "69842-220",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "SENNOSIDES",
"proprietary_name": "SENNOSIDES",
"active_ingred_unit": "mg/1",
"application_number": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "SENNOSIDES",
"start_marketing_date": "20180703",
"active_numerator_strength": "8.6"
}Access this data programmatically
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