stool softener

Generic: docusate sodium

Labeler: h e b
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name stool softener
Generic Name docusate sodium
Labeler h e b
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

docusate sodium 250 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-879
Product ID 37808-879_ad646c69-031a-4194-a32c-df17be7e08e8
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2021-03-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808879
Hyphenated Format 37808-879

Supplemental Identifiers

RxCUI
1245468
UPC
0041220541706
UNII
F05Q2T2JA0

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 (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 140 CAPSULE, LIQUID FILLED in 1 BOTTLE (37808-879-14)
source: ndc

Packages (1)

Ingredients (1)

docusate sodium (250 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ad646c69-031a-4194-a32c-df17be7e08e8", "openfda": {"upc": ["0041220541706"], "unii": ["F05Q2T2JA0"], "rxcui": ["1245468"], "spl_set_id": ["1dd2be7e-bdca-4e43-b853-3ed10b636632"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "140 CAPSULE, LIQUID FILLED in 1 BOTTLE (37808-879-14)", "package_ndc": "37808-879-14", "marketing_start_date": "20210326"}], "brand_name": "Stool Softener", "product_id": "37808-879_ad646c69-031a-4194-a32c-df17be7e08e8", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "37808-879", "generic_name": "Docusate Sodium", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "250 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210326", "listing_expiration_date": "20261231"}