stool softener laxative

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

docusate sodium 100 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-853
Product ID 37808-853_8efe0b7f-a064-40b6-87f8-14713d25b49a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2021-10-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808853
Hyphenated Format 37808-853

Supplemental Identifiers

RxCUI
1115005
UPC
0041220569304
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 laxative (source: ndc)
Generic Name docusate sodium (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (37808-853-30)
source: ndc

Packages (1)

Ingredients (1)

docusate sodium (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8efe0b7f-a064-40b6-87f8-14713d25b49a", "openfda": {"upc": ["0041220569304"], "unii": ["F05Q2T2JA0"], "rxcui": ["1115005"], "spl_set_id": ["84116db2-a7b7-460a-a5e5-8558bd424781"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (37808-853-30)", "package_ndc": "37808-853-30", "marketing_start_date": "20211029"}], "brand_name": "Stool Softener Laxative", "product_id": "37808-853_8efe0b7f-a064-40b6-87f8-14713d25b49a", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "37808-853", "generic_name": "DOCUSATE SODIUM", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener Laxative", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "100 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211029", "listing_expiration_date": "20261231"}