pedia-lax

Generic: docusate sodium

Labeler: c.b. fleet company, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pedia-lax
Generic Name docusate sodium
Labeler c.b. fleet company, inc.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

docusate sodium 50 mg/15mL

Manufacturer
C.B. Fleet Company, Inc.

Identifiers & Regulatory

Product NDC 0132-0113
Product ID 0132-0113_6c2dec84-5645-49f0-a3c2-882f4e28d67e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2023-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01320113
Hyphenated Format 0132-0113

Supplemental Identifiers

RxCUI
1088245 1088249
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 pedia-lax (source: ndc)
Generic Name docusate sodium (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/15mL
source: ndc
Packaging
  • 118 mL in 1 CARTON (0132-0113-24)
source: ndc

Packages (1)

0132-0113-24 118 mL in 1 CARTON (0132-0113-24)

Ingredients (1)

docusate sodium (50 mg/15mL)

Linked Drug Pages (1)

Pedia-Lax ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6c2dec84-5645-49f0-a3c2-882f4e28d67e", "openfda": {"unii": ["F05Q2T2JA0"], "rxcui": ["1088245", "1088249"], "spl_set_id": ["0e908bea-ebab-44e7-919c-90002e6f5d42"], "manufacturer_name": ["C.B. Fleet Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 CARTON (0132-0113-24)", "package_ndc": "0132-0113-24", "marketing_start_date": "20230228"}], "brand_name": "Pedia-Lax", "product_id": "0132-0113_6c2dec84-5645-49f0-a3c2-882f4e28d67e", "dosage_form": "LIQUID", "product_ndc": "0132-0113", "generic_name": "Docusate Sodium", "labeler_name": "C.B. Fleet Company, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pedia-Lax", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/15mL"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230228", "listing_expiration_date": "20261231"}