Rite Aid Fiber Therapy
NDC Package 11822-5151-4

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Rite Aid Fiber Therapy is put one dose into an empty glass. Marketed by Rite Aid Corporation, this product is identified by NDC 11822-5151 and is authorized under FDA application part334.

Identification & Billing

NDC Package Code
11822-5151-4
Package Description
660 g in 1 CANISTER
Product Code
11822-5151
11-Digit Billing Format
11822515104
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Rite Aid Fiber Therapy
Dosage Form
-
Usage Information
Put one dose into an empty glass. Mix this product (child or adult dose) with at least 8 ounces (a full glass) of water or other fluid. Taking this product without enough liquid may cause choking. See choking warning. Stir briskly and drink promptly. If mixture thickness, add more liquid and stir.Adults 12 years & older:1 rounded TEASPOON in 8 ounces of liquid at the signs of irregularity. Can be taken up to 3 times daily. Generally produces effect in 12-72 hours.Children 6-11 yrs:½ adult dose in 8 ounces of liquid, up to 3 times dailyUnder 6 yrs:Consult a doctorBulk-forming fibers like psyllium husk may affect how well other medicines work. If you are taking a prescription medicine by mouth, take this product at least 2 hours before or 2 hours after the prescribed medicine. New Users: Start with 1 serving per day; gradually increase to desired daily intake. You may initially experience changes in bowel habits or minor bloating, as your body adjusts to increased fiber intake.

Regulatory & Marketing

Labeler Name
Rite Aid Corporation
FDA Application #
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
03-13-2019
Listing Expiration
12-31-2022
Exclude Flag
I
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 11822-5151-4 identifies a specific commercial package of 660 g in 1 canister of Rite Aid Fiber Therapy, labeled by Rite Aid Corporation. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Rite Aid Corporation on March 13, 2019. The current certification is valid through December 31, 2022.

How is this Rite Aid Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11822515104. 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)
11822-5151-4
11-Digit CMS (5-4-2)
11822-5151-04

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