Iodine And Potassium Iodide Liquid
NDC Package 0395-2775-16

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 an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Iodine And Potassium Iodide liquids is a human prescription drug. This formulation utilizes a liquid delivery system. Marketed by Humco Holding Group, Inc., this product is identified by NDC 0395-2775.

Identification & Billing

NDC Package Code
0395-2775-16
Package Description
473 mL in 1 BOTTLE, PLASTIC
Product Code
0395-2775
11-Digit Billing Format
00395277516
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Units Per Package
473 ML

Clinical Specifications

Proprietary Name
Iodine And Potassium Iodide
Non-Proprietary Name
Iodine And Potassium Iodide
Substance Name
Iodine; Potassium Iodide
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Active Ingredient(s)

Regulatory & Marketing

Labeler Name
Humco Holding Group, Inc.
Product Type
Human Prescription Drug
Marketing Category
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date
01-01-2008
Listing Expiration
12-31-2026
Exclude Flag
N
Unfinished Product
Yes
Sample Package
N/A

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 0395-2775-16 identifies a specific commercial package of 473 ml in 1 bottle, plastic of Iodine And Potassium Iodide (UNFINISHED drug), a human prescription drug labeled by Humco Holding Group, Inc.. This product is billed per "ML" milliliter and contains an estimated amount of 473 billable units per package. This liquid is formulated for use and contains iodine; potassium iodide 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 Humco Holding Group, Inc. on January 01, 2008. The current certification is valid through December 31, 2026.

How is this Humco Holding Group, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00395277516. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 473 total billable units per package. 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 (4-4-2)
0395-2775-16
11-Digit CMS (5-4-2)
00395-2775-16

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