stool softener

Generic: docusate sodium sennosides

Labeler: quality choice (chain drug marketing association)
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name stool softener
Generic Name docusate sodium sennosides
Labeler quality choice (chain drug marketing association)
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
QUALITY CHOICE (Chain Drug Marketing Association)

Identifiers & Regulatory

Product NDC 83324-136
Product ID 83324-136_f77811f2-a305-411a-a942-0ba744c6d5b8
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2024-07-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83324136
Hyphenated Format 83324-136

Supplemental Identifiers

RxCUI
998740
UPC
0635515997165
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 (source: ndc)
Generic Name docusate sodium sennosides (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
  • 8.6 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (83324-136-01)
source: ndc

Packages (1)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f77811f2-a305-411a-a942-0ba744c6d5b8", "openfda": {"upc": ["0635515997165"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["d4128fbd-32ba-4d2e-ae1a-cbe438f5b39b"], "manufacturer_name": ["QUALITY CHOICE (Chain Drug Marketing Association)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (83324-136-01)", "package_ndc": "83324-136-01", "marketing_start_date": "20240731"}], "brand_name": "Stool Softener", "product_id": "83324-136_f77811f2-a305-411a-a942-0ba744c6d5b8", "dosage_form": "TABLET", "product_ndc": "83324-136", "generic_name": "Docusate Sodium Sennosides", "labeler_name": "QUALITY CHOICE (Chain Drug Marketing Association)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/1"}, {"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240731", "listing_expiration_date": "20261231"}