Heb Fiber Therapy Powder, For Solution
NDC Package 37808-716-16

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Heb Fiber Therapy (methylcellulose) powders is •MIX THIS PRODUCT (CHILD OR ADULT DOSE) WITH AT LEAST 8 OUNCES (A FULL GLASS) OF WATER OR OTHER FLUID. This formulation utilizes a powder, for solution delivery system. Marketed by Heb, this product is identified by NDC 37808-716 and is authorized under FDA application M007.

Identification & Billing

NDC Package Code
37808-716-16
Package Description
479 g in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
37808071616
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Heb Fiber Therapy
Non-Proprietary Name
Methylcellulose
Substance Name
Methylcellulose (4000 Mpa.s)
Dosage Form
Powder, For Solution - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a solution.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
•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•use product at the first sign of constipation or irregularity•put one dose in a full glass of cold water•stir briskly and drink promptly•drinking another glass of water is helpfulAgeDoseadults & children 12 years of age and overstart with 1 heaping tablespoon. Increase as needed, 1 heaping tablespoon at a time, up to 3 times per day.children 6 - 11 years of agestart with 2.5 level teaspoons. Increase as needed, 2.5 level teaspoons at a time, up to 3 times per day.children under 6 years of ageconsult a physician

Regulatory & Marketing

Labeler Name
Heb
Product Type
Human Otc Drug
FDA Application #
M007
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-25-2019
Listing Expiration
12-31-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 37808-716-16 identifies a specific commercial package of 479 g in 1 bottle, plastic of Heb Fiber Therapy, a human over the counter drug labeled by Heb. This powder, for solution is formulated for oral use and contains methylcellulose (4000 mpa.s) 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 Heb on April 25, 2019. The current certification is valid through December 31, 2026.

How is this Heb product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 37808071616. 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)
37808-716-16
11-Digit CMS (5-4-2)
37808-0716-16

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