stool softener plus stimulant laxative

Generic: docusate sodium and sennosides

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

Drug Facts

Product Profile

Brand Name stool softener plus stimulant laxative
Generic Name docusate sodium and sennosides
Labeler safeway, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
Safeway, Inc.

Identifiers & Regulatory

Product NDC 21130-878
Product ID 21130-878_047a9d14-a528-4ac5-8a25-ed236e4a3baa
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2020-09-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 21130878
Hyphenated Format 21130-878

Supplemental Identifiers

RxCUI
998740
UPC
0321130778899
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 stool softener plus stimulant laxative (source: ndc)
Generic Name docusate sodium and sennosides (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
  • 8.6 mg/1
source: ndc
Packaging
  • 200 TABLET in 1 BOTTLE, PLASTIC (21130-878-20)
source: ndc

Packages (1)

21130-878-20 200 TABLET in 1 BOTTLE, PLASTIC (21130-878-20)

Ingredients (2)

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

Linked Drug Pages (1)

Stool Softener Plus Stimulant Laxative ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "047a9d14-a528-4ac5-8a25-ed236e4a3baa", "openfda": {"upc": ["0321130778899"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["6bc9ea37-31b8-4a6d-9b2d-2c80bad4f30d"], "manufacturer_name": ["Safeway, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE, PLASTIC (21130-878-20)", "package_ndc": "21130-878-20", "marketing_start_date": "20200930"}], "brand_name": "Stool Softener Plus Stimulant Laxative", "product_id": "21130-878_047a9d14-a528-4ac5-8a25-ed236e4a3baa", "dosage_form": "TABLET", "product_ndc": "21130-878", "generic_name": "docusate sodium and sennosides", "labeler_name": "Safeway, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener", "brand_name_suffix": "Plus Stimulant Laxative", "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": "20200930", "listing_expiration_date": "20261231"}