NDC Package 69842-089-52 Womens Gentle Laxative

Bisacodyl Tablet, Coated Oral - View Billable Units, 11-Digit Format, RxNorm

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:
69842-089-52
Package Description:
25 TABLET, COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Womens Gentle Laxative
Non-Proprietary Name:
Bisacodyl
Substance Name:
Bisacodyl
Usage Information:
Bisacodyl is used to treat constipation. It may also be used to clean out the intestines before a bowel examination/surgery. Bisacodyl is known as a stimulant laxative. It works by increasing the movement of the intestines, helping the stool to come out.
11-Digit NDC Billing Format:
69842008952
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
25 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 308753 - bisacodyl 5 MG Delayed Release Oral Tablet
  • RxCUI: 308753 - bisacodyl 5 MG Enteric Coated Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Cvs Health Corp
    Dosage Form:
    Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    part334
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    08-24-2020
    Listing Expiration Date:
    12-31-2024
    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 69842-089-52?

    The NDC Packaged Code 69842-089-52 is assigned to a package of 25 tablet, coated in 1 blister pack of Womens Gentle Laxative, a human over the counter drug labeled by Cvs Health Corp. The product's dosage form is tablet, coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 25 billable units per package.

    Is NDC 69842-089 included in the NDC Directory?

    Yes, Womens Gentle Laxative with product code 69842-089 is active and included in the NDC Directory. The product was first marketed by Cvs Health Corp on August 24, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 69842-089-52?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 25.

    What is the 11-digit format for NDC 69842-089-52?

    The 11-digit format is 69842008952. 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 5-3-2 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
    5-3-269842-089-525-4-269842-0089-52