Chicory Ginger Bitters Liquid
NDC Package 48951-3251-3
Package Information
Chicory Ginger Bitters liquids is directions: FOR ORAL USE ONLY. This formulation utilizes a liquid delivery system. Marketed by Uriel Pharmacy, Inc., this product is identified by NDC 48951-3251.
Identification & Billing
Clinical Specifications
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Vegetable Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 48951 - Uriel Pharmacy, Inc.
- 48951-3251 - Chicory Ginger Bitters
- 48951-3251-3 - 60 mL in 1 BOTTLE, GLASS
- 48951-3251 - Chicory Ginger Bitters
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.
Other Available Packages
The following commercial packages are registered under the same Product NDC (48951-3251). Click a package code to view its specific billing and regulatory data.
* 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 48951-3251-3 identifies a specific commercial package of 60 ml in 1 bottle, glass of Chicory Ginger Bitters, a human over the counter drug labeled by Uriel Pharmacy, Inc.. This liquid is formulated for oral use and contains acorus calamus root; black pepper; chelidonium majus; cichorium intybus whole; gentiana lutea root; ginger; milk thistle; turmeric; wormwood 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: 48951325103. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.