stool softener and stimulant laxative
Generic: docusate sodium and sennosides
Labeler: target corporationDrug Facts
Product Profile
Brand Name
stool softener and stimulant laxative
Generic Name
docusate sodium and sennosides
Labeler
target corporation
Dosage Form
TABLET
Routes
Active Ingredients
docusate sodium 50 mg/1, sennosides 8.6 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
11673-209
Product ID
11673-209_203f9749-cfcf-667a-e063-6394a90af48c
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M007
Listing Expiration
2026-12-31
Marketing Start
2019-04-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11673209
Hyphenated Format
11673-209
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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 and stimulant laxative (source: ndc)
Generic Name
docusate sodium and sennosides (source: ndc)
Application Number
M007 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
- 8.6 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (11673-209-01)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "203f9749-cfcf-667a-e063-6394a90af48c", "openfda": {"upc": ["0349483097016"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["7cac99da-8d89-0aee-e053-2991aa0a0fd9"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (11673-209-01)", "package_ndc": "11673-209-01", "marketing_start_date": "20190510"}], "brand_name": "STOOL SOFTENER AND STIMULANT LAXATIVE", "product_id": "11673-209_203f9749-cfcf-667a-e063-6394a90af48c", "dosage_form": "TABLET", "product_ndc": "11673-209", "generic_name": "DOCUSATE SODIUM AND SENNOSIDES", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "STOOL SOFTENER AND 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": "20190410", "listing_expiration_date": "20261231"}