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  5. NDC Package Code: 0132-0113-24 Pedia-lax

NDC Package 0132-0113-24 Pedia-lax

Docusate Sodium Liquid Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0132-0113-24
Package Description:
118 mL in 1 CARTON
Product Code:
0132-0113
Proprietary Name:
Pedia-lax
Non-Proprietary Name:
Docusate Sodium
Substance Name:
Docusate Sodium
Usage Information:
This medication is used for a short time to treat occasional constipation. It is a laxative (osmotic-type) that is thought to work by drawing water into the intestines, an effect that helps to cause movement of the intestines. This medication is also used to treat symptoms caused by too much stomach acid such as heartburn, upset stomach, or indigestion. It is an antacid that works by lowering the amount of acid in the stomach.
11-Digit NDC Billing Format:
00132011324
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
C.b. Fleet Company, Inc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
DOCUSATE SODIUM 50 mg/15mL
Sample Package:
No
FDA Application Number:
M007
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
02-28-2023
Listing Expiration Date:
12-31-2025
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0132-0113-24?

The NDC Packaged Code 0132-0113-24 is assigned to a package of 118 ml in 1 carton of Pedia-lax, a human over the counter drug labeled by C.b. Fleet Company, Inc.. The product's dosage form is liquid and is administered via oral form.

Is NDC 0132-0113 included in the NDC Directory?

Yes, Pedia-lax with product code 0132-0113 is active and included in the NDC Directory. The product was first marketed by C.b. Fleet Company, Inc. on February 28, 2023 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0132-0113-24?

The 11-digit format is 00132011324. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
4-4-20132-0113-245-4-200132-0113-24