Stool Softener Laxative Capsule, Liquid Filled
NDC Package 17856-7281-9

11-digit billing NDC: 17856728109
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Stool Softener Laxative (docusate sodium) capsules is adults and children 12 years of age and over: take 1 softgel daily or as directed by a doctorchildren under 12 years of age: ask a doctor. This formulation utilizes a capsule, liquid filled delivery system. Marketed by Atlantic Biologicals Corp., this product is identified by NDC 17856-7281 and is authorized under FDA application M.

Identification & Billing

NDC Package Code
17856-7281-9
Package Description
99 POUCH in 1 BOX, UNIT-DOSE / 1 CAPSULE, LIQUID FILLED in 1 POUCH
Product Code
17856-7281
11-Digit Billing Format
17856728109
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Stool Softener Laxative
Non-Proprietary Name
Docusate Sodium
Substance Name
Docusate Sodium
Dosage Form
Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
DOCUSATE SODIUM 250 mg/1
Usage Information
Adults and children 12 years of age and over: take 1 softgel daily or as directed by a doctorchildren under 12 years of age: ask a doctor

Regulatory & Marketing

Labeler Name
Atlantic Biologicals Corp.
Product Type
Human Otc Drug
FDA Application #
M
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-14-2022
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (17856-7281). Click a package code to view its specific billing and regulatory data.

17856-7281-1
100 POUCH in 1 BOX, UNIT-DOSE / 1 CAPSULE, LIQUID FILLED in 1 POUCH

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 17856-7281-9 identifies a specific commercial package of 99 pouch in 1 box, unit-dose / 1 capsule, liquid filled in 1 pouch of Stool Softener Laxative, a human over the counter drug labeled by Atlantic Biologicals Corp.. This capsule, liquid filled is formulated for oral use and contains docusate sodium as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Atlantic Biologicals Corp. on October 14, 2022. The current certification is valid through December 31, 2027.

How is this Atlantic Biologicals Corp. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 17856728109. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
17856-7281-9
11-Digit CMS (5-4-2)
17856-7281-09

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.