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  5. NDC Package Code: 85631-003-01 Gout Relief 3310-s

NDC Package 85631-003-01 Gout Relief 3310-s

Celery Seed,Medicago Sativa Whole, Chicory Root Capsule Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
85631-003-01
Package Description:
60 CAPSULE in 1 BOX / 1.3 g in 1 CAPSULE
Product Code:
85631-003
Proprietary Name:
Gout Relief 3310-s
Non-Proprietary Name:
Celery Seed, Medicago Sativa Whole, Chicory Root
Substance Name:
Buckwheat; Celery Seed; Chicory Root; Glucosamine Hydrochloride; Licorice; Medicago Sativa Whole; Morus Alba Leaf; Puerarin; Sodium Chloride; Tea Leaf
Usage Information:
Dissolved CrystallizationKidney StoneGallstone< Urinary Calculus
11-Digit NDC Billing Format:
85631000301
Product Type:
Human Otc Drug
Labeler Name:
Bispit Canada Ltd.
Dosage Form:
Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
07-28-2025
Listing Expiration Date:
12-31-2026
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 85631-003-01?

The NDC Packaged Code 85631-003-01 is assigned to a package of 60 capsule in 1 box / 1.3 g in 1 capsule of Gout Relief 3310-s, a human over the counter drug labeled by Bispit Canada Ltd.. The product's dosage form is capsule and is administered via oral form.

Is NDC 85631-003 included in the NDC Directory?

Yes, Gout Relief 3310-s with product code 85631-003 is active and included in the NDC Directory. The product was first marketed by Bispit Canada Ltd. on July 28, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 85631-003-01?

The 11-digit format is 85631000301. 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
5-3-285631-003-015-4-285631-0003-01