1. Home
  2. Labeler Index
  3. Perrigo Direct, Inc.
  4. 50804-088
  5. NDC Package Code: 50804-088-10 Iodine

NDC Package 50804-088-10 Iodine

Liquid Topical - 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:
50804-088-10
Package Description:
30 mL in 1 BOTTLE, PLASTIC
Product Code:
50804-088
Proprietary Name:
Iodine
Non-Proprietary Name:
Iodine
Substance Name:
Alcohol; Iodine; Sodium Iodide
Usage Information:
Clean the affected areaapply a small amount on the area 1 to 3 times dailymay be covered with a sterile bandageif bandaged, let dry first
11-Digit NDC Billing Format:
50804008810
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
30 ML
Product Type:
Human Otc Drug
Labeler Name:
Perrigo Direct, 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):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • ALCOHOL 470 mg/mL
  • IODINE 20 mg/mL
  • SODIUM IODIDE 20.4 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    part333A
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    11-08-2008
    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 50804-088-10?

    The NDC Packaged Code 50804-088-10 is assigned to a package of 30 ml in 1 bottle, plastic of Iodine, a human over the counter drug labeled by Perrigo Direct, Inc.. The product's dosage form is liquid and is administered via topical form.This product is billed per "ML" milliliter and contains an estimated amount of 30 billable units per package.

    Is NDC 50804-088 included in the NDC Directory?

    Yes, Iodine with product code 50804-088 is active and included in the NDC Directory. The product was first marketed by Perrigo Direct, Inc. on November 08, 2008 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 NDC billing unit for package 50804-088-10?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 30.

    What is the 11-digit format for NDC 50804-088-10?

    The 11-digit format is 50804008810. 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
    5-3-250804-088-105-4-250804-0088-10