stimulant laxative plus stool softener

Generic: docusate sodium 50 mg and sennosides 8.6 mg

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name stimulant laxative plus stool softener
Generic Name docusate sodium 50 mg and sennosides 8.6 mg
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7674
Product ID 68788-7674_a3516560-2440-4bb0-bf1d-3970a07b598c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number part334
Listing Expiration 2026-12-31
Marketing Start 2020-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887674
Hyphenated Format 68788-7674

Supplemental Identifiers

RxCUI
998740
UNII
F05Q2T2JA0 3FYP5M0IJX

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 stimulant laxative plus stool softener (source: ndc)
Generic Name docusate sodium 50 mg and sennosides 8.6 mg (source: ndc)
Application Number part334 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
  • 8.6 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7674-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7674-6)
source: ndc

Packages (2)

68788-7674-1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7674-1) 68788-7674-6 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7674-6)

Ingredients (2)

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

Linked Drug Pages (1)

Stimulant Laxative Plus Stool Softener ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a3516560-2440-4bb0-bf1d-3970a07b598c", "openfda": {"unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["b25b8a28-5e00-4a20-9ca3-7ed494fc4540"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7674-1)", "package_ndc": "68788-7674-1", "marketing_start_date": "20200228"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7674-6)", "package_ndc": "68788-7674-6", "marketing_start_date": "20200228"}], "brand_name": "Stimulant Laxative Plus Stool Softener", "product_id": "68788-7674_a3516560-2440-4bb0-bf1d-3970a07b598c", "dosage_form": "TABLET, FILM COATED", "product_ndc": "68788-7674", "generic_name": "Docusate Sodium 50 mg and Sennosides 8.6 mg", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stimulant Laxative Plus Stool Softener", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/1"}, {"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "part334", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200228", "listing_expiration_date": "20261231"}