De La Cruz Decolorized Iodine Liquid
NDC Package 24286-1529-8

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

Package Information

De La Cruz Decolorized Iodine (ethyl alcohol) liquids is clean the affected area. This formulation utilizes a liquid delivery system. Marketed by Dlc Laboratories, Inc., this product is identified by NDC 24286-1529 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
24286-1529-8
Package Description
59 mL in 1 BOTTLE, PLASTIC
Product Code
24286-1529
11-Digit Billing Format
24286152908

Clinical Specifications

Proprietary Name
De La Cruz Decolorized Iodine
Non-Proprietary Name
Ethyl Alcohol
Substance Name
Alcohol
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
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 .45 mL/mL
Usage Information
Clean the affected area. Apply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. Allow affected area to dry completely, before applying sterile bandage.

Regulatory & Marketing

Labeler Name
Dlc Laboratories, Inc.
Product Type
Human Otc Drug
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-25-1998
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 24286-1529-8 identifies a specific commercial package of 59 ml in 1 bottle, plastic of De La Cruz Decolorized Iodine, a human over the counter drug labeled by Dlc Laboratories, Inc.. This liquid is formulated for topical use and contains alcohol 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 Dlc Laboratories, Inc. on March 25, 1998. The current certification is valid through December 31, 2026.

How is this Dlc Laboratories, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 24286152908. 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)
24286-1529-8
11-Digit CMS (5-4-2)
24286-1529-08

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