senokot-s

Generic: standardized senna concentrate and docusate sodium

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

Drug Facts

Product Profile

Brand Name senokot-s
Generic Name standardized senna concentrate and docusate sodium
Labeler atlantis consumer healthcare, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

docusate sodium 50 mg/1, sennosides 8.6 mg/1

Manufacturer
Atlantis Consumer Healthcare, Inc.

Identifiers & Regulatory

Product NDC 67618-310
Product ID 67618-310_c7d88a4f-4a36-445a-8615-099c0fd6f1d0
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 1974-10-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67618310
Hyphenated Format 67618-310

Supplemental Identifiers

RxCUI
998740 1248015
UPC
0367618310601
UNII
F05Q2T2JA0 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-s (source: ndc)
Generic Name standardized senna concentrate and docusate sodium (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
  • 8.6 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (67618-310-01) / 10 TABLET in 1 BLISTER PACK
  • 1 BOTTLE, PLASTIC in 1 CARTON (67618-310-30) / 30 TABLET in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (67618-310-60) / 60 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (3)

67618-310-01 1 BLISTER PACK in 1 CARTON (67618-310-01) / 10 TABLET in 1 BLISTER PACK 67618-310-30 1 BOTTLE, PLASTIC in 1 CARTON (67618-310-30) / 30 TABLET in 1 BOTTLE, PLASTIC 67618-310-60 1 BOTTLE, PLASTIC in 1 CARTON (67618-310-60) / 60 TABLET in 1 BOTTLE, PLASTIC

Ingredients (2)

docusate sodium (50 mg/1) sennosides (8.6 mg/1)

Linked Drug Pages (1)

Senokot-S ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c7d88a4f-4a36-445a-8615-099c0fd6f1d0", "openfda": {"upc": ["0367618310601"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740", "1248015"], "spl_set_id": ["c24cdc5e-62e0-41a6-8afb-512202a569f4"], "manufacturer_name": ["Atlantis Consumer Healthcare, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (67618-310-01)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "67618-310-01", "marketing_start_date": "19741001"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (67618-310-30)  / 30 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "67618-310-30", "marketing_start_date": "19741001"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (67618-310-60)  / 60 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "67618-310-60", "marketing_start_date": "19741001"}], "brand_name": "Senokot-S", "product_id": "67618-310_c7d88a4f-4a36-445a-8615-099c0fd6f1d0", "dosage_form": "TABLET", "product_ndc": "67618-310", "generic_name": "standardized senna concentrate and docusate sodium", "labeler_name": "Atlantis Consumer Healthcare, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Senokot-S", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/1"}, {"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19741001", "listing_expiration_date": "20261231"}