Stibium 6x Powder
NDC Package 48951-8401-4

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

Package Information

Stibium 6x powders is directions: FOR ORAL USE ONLY. This formulation utilizes a powder delivery system. Marketed by Uriel Pharmacy Inc., this product is identified by NDC 48951-8401.

Identification & Billing

NDC Package Code
48951-8401-4
Package Description
50 g in 1 BOTTLE, GLASS
Product Code
48951-8401
11-Digit Billing Format
48951840104

Clinical Specifications

Proprietary Name
Stibium 6x
Non-Proprietary Name
Stibium 6x
Substance Name
Antimony
Dosage Form
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
ANTIMONY 6 [hp_X]/g
Usage Information
Directions: FOR ORAL USE ONLY.

Regulatory & Marketing

Labeler Name
Uriel Pharmacy Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
09-01-2009
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 48951-8401-4 identifies a specific commercial package of 50 g in 1 bottle, glass of Stibium 6x, a human over the counter drug labeled by Uriel Pharmacy Inc.. This powder is formulated for oral use and contains antimony 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 Uriel Pharmacy Inc. on September 01, 2009. The current certification is valid through December 31, 2026.

How is this Uriel Pharmacy Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 48951840104. 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)
48951-8401-4
11-Digit CMS (5-4-2)
48951-8401-04

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