docusate sodium

Generic: docusate sodium

Labeler: safecor health, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name docusate sodium
Generic Name docusate sodium
Labeler safecor health, llc
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

docusate sodium 50 mg/5mL

Manufacturer
Safecor Health, LLC

Identifiers & Regulatory

Product NDC 48433-220
Product ID 48433-220_3b918dfb-629d-4eef-ba71-d2ee2f97747f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M334
Listing Expiration 2026-12-31
Marketing Start 2021-09-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 48433220
Hyphenated Format 48433-220

Supplemental Identifiers

RxCUI
1248119
UPC
0348433220405
UNII
F05Q2T2JA0

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 docusate sodium (source: ndc)
Generic Name docusate sodium (source: ndc)
Application Number M334 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/5mL
source: ndc
Packaging
  • 10 mL in 1 CUP, UNIT-DOSE (48433-220-10)
source: ndc

Packages (1)

48433-220-10 10 mL in 1 CUP, UNIT-DOSE (48433-220-10)

Ingredients (1)

docusate sodium (50 mg/5mL)

Linked Drug Pages (1)

DOCUSATE SODIUM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3b918dfb-629d-4eef-ba71-d2ee2f97747f", "openfda": {"upc": ["0348433220405"], "unii": ["F05Q2T2JA0"], "rxcui": ["1248119"], "spl_set_id": ["efe4bf81-fb99-4755-aa23-4f8df5973be8"], "manufacturer_name": ["Safecor Health, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 CUP, UNIT-DOSE (48433-220-10)", "package_ndc": "48433-220-10", "marketing_start_date": "20210901"}], "brand_name": "DOCUSATE SODIUM", "product_id": "48433-220_3b918dfb-629d-4eef-ba71-d2ee2f97747f", "dosage_form": "LIQUID", "product_ndc": "48433-220", "generic_name": "DOCUSATE SODIUM", "labeler_name": "Safecor Health, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DOCUSATE SODIUM", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/5mL"}], "application_number": "M334", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210901", "listing_expiration_date": "20261231"}