United States · FDA National Drug Code directory

Pedia-Lax

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0132-0113_6c2dec84-5645-49f0-a3c2-882f4e28d67e
Product NDC
0132-0113
Form
LIQUID
Composition / generic term
Docusate Sodium
Labeler
C.B. Fleet Company, Inc.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20230228
Source listing expiry
20261231

Source-listed ingredients

  • DOCUSATE SODIUM — 50 mg/15mL

These values do not establish equivalence or a dose recommendation.

Packages

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

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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