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United States · US · US:67618-310_c7d88a4f-4a36-445a-8615-099c0fd6f1d0

Senokot-S

UNIISPLATC A06AA

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerAtlantis Consumer Healthcare, Inc.
CountryUS (United States)
ATC codeA06AA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    6761831001
    1 BLISTER PACK in 1 CARTON (67618-310-01) / 10 TABLET in 1 BLISTER PACK
  • ndc11
    6761831030
    1 BOTTLE, PLASTIC in 1 CARTON (67618-310-30) / 30 TABLET in 1 BOTTLE, PLASTIC
  • ndc11
    6761831060
    1 BOTTLE, PLASTIC in 1 CARTON (67618-310-60) / 60 TABLET in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)
F05Q2T2JA0
DOCUSATE SODIUM
RxCUI 71722
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "F05Q2T2JA0",
    "rxcui": "71722",
    "inchikey": "APSBXTVYXVQYAB-UHFFFAOYSA-M",
    "display_name": "DOCUSATE SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "c24cdc5e-62e0-41a6-8afb-512202a569f4": {
      "match": "brand_token",
      "title": "SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [ATLANTIS CONSUMER HEALTHCARE, INC.]",
      "spl_version": "11",
      "published_date": "2025-12-31"
    }
  },
  "productid": "67618-310_c7d88a4f-4a36-445a-8615-099c0fd6f1d0",
  "productndc": "67618-310",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DOCUSATE SODIUM; SENNOSIDES",
  "proprietary_name": "Senokot-S",
  "active_ingred_unit": "mg/1; mg/1",
  "application_number": "M007",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "standardized senna concentrate and docusate sodium",
  "start_marketing_date": "19741001",
  "active_numerator_strength": "50; 8.6"
}

Related drugs

Other records sharing ATC code A06AA.

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