Mosquito Repellent
NDC Package 84445-003-01

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 EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Mosquito Repellent is a medication used as Insect Repellents. Marketed by Shenzhen Furuizhilian Keji Co., Ltd., this product is identified by NDC 84445-003 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
84445-003-01
Package Description
100 mL in 1 BOTTLE, SPRAY
Product Code
84445-003
11-Digit Billing Format
84445000301

Clinical Specifications

Proprietary Name
Mosquito Repellent
Dosage Form
-
Usage Information
This product is used as Insect Repellents. Make sure the application area is clean and dry. Spray on the application area, be careful not to spray into the mouth or nose

Regulatory & Marketing

Labeler Name
Shenzhen Furuizhilian Keji Co., Ltd.
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-11-2024
Listing Expiration
12-31-2025
Exclude Flag
I
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 84445-003-01 identifies a specific commercial package of 100 ml in 1 bottle, spray of Mosquito Repellent, labeled by Shenzhen Furuizhilian Keji Co., Ltd.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Shenzhen Furuizhilian Keji Co., Ltd. on July 11, 2024. The current certification is valid through December 31, 2025.

How is this Shenzhen Furuizhilian Keji Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84445000301. 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)
84445-003-01
11-Digit CMS (5-4-2)
84445-0003-01

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