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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

  • ndc11
    6984222008
    500 TABLET, FILM COATED in 1 BOTTLE (69842-220-08)
  • ndc11
    6984222025
    250 TABLET, FILM COATED in 1 BOTTLE (69842-220-25)
  • ndc11
    6984222050
    1 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"
}

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