Senokot

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerAtlantis Consumer Healthcare, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
6761830010
1 BOTTLE, PLASTIC in 1 CARTON (67618-300-10) / 100 TABLET in 1 BOTTLE, PLASTIC
ndc11
6761830020
2 BLISTER PACK in 1 CARTON (67618-300-20) / 10 TABLET in 1 BLISTER PACK
ndc11
6761830050
1 BOTTLE, PLASTIC in 1 CARTON (67618-300-50) / 50 TABLET in 1 BOTTLE, PLASTIC

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": "67618-300_fd1324ab-ef79-42ee-b960-9b032a3a4af2",
  "productndc": "67618-300",
  "dosage_form": "TABLET",
  "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": "19560601",
  "active_numerator_strength": "8.6"
}

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