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  5. NDC Package Code: 66096-166-02 Kali Iodatum 1x

NDC Package 66096-166-02 Kali Iodatum 1x

Kali Iodatum. Liquid 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:
66096-166-02
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
66096-166
Proprietary Name:
Kali Iodatum 1x
Non-Proprietary Name:
Kali Iodatum.
Substance Name:
Potassium Iodide
Usage Information:
Potassium iodide is used to loosen and break up mucus in the airways. This helps you cough up the mucus so you can breathe more easily if you have long-term lung problems (e.g., asthma, chronic bronchitis, emphysema). This medication is known as an expectorant. Potassium iodide is also used along with antithyroid medicines to prepare the thyroid gland for surgical removal, to treat certain overactive thyroid conditions (hyperthyroidism), and to protect the thyroid in a radiation exposure emergency. It works by shrinking the size of the thyroid gland and decreasing the amount of thyroid hormones produced. In a radiation emergency, potassium iodide blocks only the thyroid from absorbing radioactive iodine, protecting it from damage and reducing the risk of thyroid cancer. Use this medication along with other emergency measures that will be recommended to you by public health and safety officials (e.g., finding safe shelter, evacuation, controlling food supply).
11-Digit NDC Billing Format:
66096016602
Product Type:
Human Otc Drug
Labeler Name:
Ohm Pharma Inc.
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.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • POTASSIUM IODIDE 1 [hp_X]/30mL
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    02-10-2016
    Listing Expiration Date:
    12-31-2024
    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 66096-166-02?

    The NDC Packaged Code 66096-166-02 is assigned to a package of 30 ml in 1 bottle, dropper of Kali Iodatum 1x, a human over the counter drug labeled by Ohm Pharma Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 66096-166 included in the NDC Directory?

    Yes, Kali Iodatum 1x with product code 66096-166 is active and included in the NDC Directory. The product was first marketed by Ohm Pharma Inc. on February 10, 2016 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 66096-166-02?

    The 11-digit format is 66096016602. 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
    5-3-266096-166-025-4-266096-0166-02