Bisacodyl Laxative Suppository
NDC Package 71457-501-12

11-digit billing NDC: 71457050112
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Bisacodyl Laxative (bisacodyl) suppositories is detach 1 suppository from the strip; remove wrapper before inserting into the rectum as follows:hold suppository with pointed end upcarefully separate tabs with fingernailslowly pull apart by pulling tabs down on both sideremove suppository from wrapper (see illustration at the right)gently remove the suppository from the wrapperlie on your side and push suppository, pointed end first, high into the rectum so it will not slip outretain it for 15 to 20 minutesDo not exceed recommended doseif suppository seems soft, place in refrigerator for short time before useAdults and children 12 years and over1 suppository once dailyChildren under 12 yearsAsk a doctor. This formulation utilizes a suppository delivery system. Marketed by Invaderm Corporation, this product is identified by NDC 71457-501 and is authorized under FDA application M007.

Identification & Billing

NDC Package Code
71457-501-12
Package Description
2 BLISTER PACK in 1 CARTON / 6 SUPPOSITORY in 1 BLISTER PACK
Product Code
71457-501
11-Digit Billing Format
71457050112
RxNorm Crosswalk
RxCUI: 198509 - bisacodyl 10 MG Rectal Suppository

Clinical Specifications

Proprietary Name
Bisacodyl Laxative
Non-Proprietary Name
Bisacodyl
Substance Name
Bisacodyl
Dosage Form
Suppository - A solid body of various weights and shapes, adapted for introduction into the rectal orifice of the human body; they usually melt, soften, or dissolve at body temperature.
Administration Route
Rectal - Administration to the rectum.
Active Ingredient(s)
BISACODYL 10 mg/1
Pharmacologic Class
Usage Information
Detach 1 suppository from the strip; remove wrapper before inserting into the rectum as follows:hold suppository with pointed end upcarefully separate tabs with fingernailslowly pull apart by pulling tabs down on both sideremove suppository from wrapper (see illustration at the right)gently remove the suppository from the wrapperlie on your side and push suppository, pointed end first, high into the rectum so it will not slip outretain it for 15 to 20 minutesDo not exceed recommended doseif suppository seems soft, place in refrigerator for short time before useAdults and children 12 years and over1 suppository once dailyChildren under 12 yearsAsk a doctor

Regulatory & Marketing

Labeler Name
Invaderm Corporation
Product Type
Human Otc Drug
FDA Application #
M007
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-01-2026
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 (71457-501). Click a package code to view its specific billing and regulatory data.

71457-501-01
17 BLISTER PACK in 1 CARTON / 6 SUPPOSITORY in 1 BLISTER PACK
71457-501-24
4 BLISTER PACK in 1 CARTON / 6 SUPPOSITORY in 1 BLISTER PACK
71457-501-50
9 BLISTER PACK in 1 CARTON / 6 SUPPOSITORY in 1 BLISTER PACK

* 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 71457-501-12 identifies a specific commercial package of 2 blister pack in 1 carton / 6 suppository in 1 blister pack of Bisacodyl Laxative, a human over the counter drug labeled by Invaderm Corporation. This suppository is formulated for rectal use and contains bisacodyl 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 Invaderm Corporation on September 01, 2026. The current certification is valid through December 31, 2027.

How is this Invaderm Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71457050112. 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 (5-3-2)
71457-501-12
11-Digit CMS (5-4-2)
71457-0501-12

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