Daycon Antibacterial Foaming Hand So Ap Liquid
NDC Package 71874-080-40

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

Package Information

Daycon Antibacterial Foaming Hand So Ap (chloroxylenol) liquids is wet handsApply a small amount of product and work into a latherRinse well and dry hands completely. This formulation utilizes a liquid delivery system. Marketed by Daycon Products Company, Inc., this product is identified by NDC 71874-080 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
71874-080-40
Package Description
1200 mL in 1 PACKAGE
Product Code
71874-080
11-Digit Billing Format
71874008040

Clinical Specifications

Proprietary Name
Daycon Antibacterial Foaming Hand So Ap
Non-Proprietary Name
Chloroxylenol
Substance Name
Chloroxylenol
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)
CHLOROXYLENOL .3 mg/100mL
Usage Information
Wet handsApply a small amount of product and work into a latherRinse well and dry hands completely

Regulatory & Marketing

Labeler Name
Daycon Products Company, Inc.
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-28-2011
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (71874-080). Click a package code to view its specific billing and regulatory data.

71874-080-42
1250 mL in 1 PACKAGE

* 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 71874-080-40 identifies a specific commercial package of 1200 ml in 1 package of Daycon Antibacterial Foaming Hand So Ap, a human over the counter drug labeled by Daycon Products Company, Inc.. This liquid is formulated for topical use and contains chloroxylenol 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 Daycon Products Company, Inc. on February 28, 2011. The current certification is valid through December 31, 2026.

How is this Daycon Products Company, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71874008040. 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 (5-3-2)
71874-080-40
11-Digit CMS (5-4-2)
71874-0080-40

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