NDC Package 17433-9884-5 Docusol Kids

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

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

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:
17433-9884-5
Package Description:
5 TUBE in 1 BOX / 5 mL in 1 TUBE (17433-9884-1)
Product Code:
Proprietary Name:
Docusol Kids
Non-Proprietary Name:
Docusate Sodium
Substance Name:
Docusate Sodium
Usage Information:
This medication is used to treat occasional constipation. Some medications and conditions can make constipation more likely. Stool softeners such as docusate are often the first method used for preventing and treating this type of constipation. Docusate is often used when straining to have a bowel movement should be avoided (e.g., after a heart attack or surgery). Docusate is a stool softener. It works by increasing the amount of water the stool absorbs in the gut, making the stool softer and easier to pass.
11-Digit NDC Billing Format:
17433988405
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Enemeez Llc Dba Summit Pharmaceuticals
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):
Rectal - Administration to the rectum.
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:
01-14-2014
End Marketing Date:
11-30-2025
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.

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Frequently Asked Questions

What is NDC 17433-9884-5?

The NDC Packaged Code 17433-9884-5 is assigned to a package of 5 tube in 1 box / 5 ml in 1 tube (17433-9884-1) of Docusol Kids, a human over the counter drug labeled by Enemeez Llc Dba Summit Pharmaceuticals. The product's dosage form is liquid and is administered via rectal form.

Is NDC 17433-9884 included in the NDC Directory?

Yes, Docusol Kids with product code 17433-9884 is active and included in the NDC Directory. The product was first marketed by Enemeez Llc Dba Summit Pharmaceuticals on January 14, 2014.

What is the NDC billing unit for package 17433-9884-5?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 17433-9884-5?

The 11-digit format is 17433988405. 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 5-4-1 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
5-4-117433-9884-55-4-217433-9884-05