senokot

Generic: standardized senna concentrate

Labeler: atlantis consumer healthcare, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name senokot
Generic Name standardized senna concentrate
Labeler atlantis consumer healthcare, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sennosides 17.2 mg/1

Manufacturer
Atlantis Consumer Healthcare, Inc.

Identifiers & Regulatory

Product NDC 67618-120
Product ID 67618-120_8319c8b6-8d3f-416d-a864-39cb879df2da
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 1988-09-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67618120
Hyphenated Format 67618-120

Supplemental Identifiers

RxCUI
602802 1039965
UPC
0367618120125 0367618120064
UNII
3FYP5M0IJX

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name senokot (source: ndc)
Generic Name standardized senna concentrate (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 17.2 mg/1
source: ndc
Packaging
  • 36 TABLET, FILM COATED in 1 BOTTLE (67618-120-06)
  • 1 BLISTER PACK in 1 CARTON (67618-120-12) / 12 TABLET, FILM COATED in 1 BLISTER PACK
  • 2 CARTON in 1 PACKAGE (67618-120-72) / 1 BOTTLE in 1 CARTON / 36 TABLET, FILM COATED in 1 BOTTLE
  • 72 TABLET, FILM COATED in 1 BOTTLE (67618-120-73)
source: ndc

Packages (4)

67618-120-06 36 TABLET, FILM COATED in 1 BOTTLE (67618-120-06) 67618-120-12 1 BLISTER PACK in 1 CARTON (67618-120-12) / 12 TABLET, FILM COATED in 1 BLISTER PACK 67618-120-72 2 CARTON in 1 PACKAGE (67618-120-72) / 1 BOTTLE in 1 CARTON / 36 TABLET, FILM COATED in 1 BOTTLE 67618-120-73 72 TABLET, FILM COATED in 1 BOTTLE (67618-120-73)

Ingredients (1)

sennosides (17.2 mg/1)

Linked Drug Pages (1)

Senokot ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8319c8b6-8d3f-416d-a864-39cb879df2da", "openfda": {"upc": ["0367618120125", "0367618120064"], "unii": ["3FYP5M0IJX"], "rxcui": ["602802", "1039965"], "spl_set_id": ["d5bf67e5-82c6-edbf-e9ec-e027fdd47c84"], "manufacturer_name": ["Atlantis Consumer Healthcare, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "36 TABLET, FILM COATED in 1 BOTTLE (67618-120-06)", "package_ndc": "67618-120-06", "marketing_start_date": "19880901"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (67618-120-12)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67618-120-12", "marketing_start_date": "19880901"}, {"sample": false, "description": "2 CARTON in 1 PACKAGE (67618-120-72)  / 1 BOTTLE in 1 CARTON / 36 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "67618-120-72", "marketing_start_date": "20240101"}, {"sample": false, "description": "72 TABLET, FILM COATED in 1 BOTTLE (67618-120-73)", "package_ndc": "67618-120-73", "marketing_start_date": "20251115"}], "brand_name": "Senokot", "product_id": "67618-120_8319c8b6-8d3f-416d-a864-39cb879df2da", "dosage_form": "TABLET, FILM COATED", "product_ndc": "67618-120", "generic_name": "standardized senna concentrate", "labeler_name": "Atlantis Consumer Healthcare, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Senokot", "active_ingredients": [{"name": "SENNOSIDES", "strength": "17.2 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19880901", "listing_expiration_date": "20261231"}