Aid And First Sting Relief Prep Pad
NDC Package 69139-203-01

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.

Aid And First Sting Relief Prep Pad is adults and children 2 years of age and older use on hands and face to clean and refresh, allow skin to air dryFor children under 2 years ask a doctor before use.Tear open packet, unfold towelltte and use to clean desired skin area, discard towelltte appropriately after use. Marketed by Yiwu Haoding Medical Co.,ltd, this product is identified by NDC 69139-203 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
69139-203-01
Package Description
1 PACKET in 1 PACKAGE / .3 g in 1 PACKET
Product Code
69139-203
11-Digit Billing Format
69139020301
RxNorm Crosswalk
  • RxCUI: 895749 - benzocaine 6 % / isopropyl alcohol 60 % Medicated Pad
  • RxCUI: 895749 - benzocaine 60 MG/ML / isopropyl alcohol 0.6 ML/ML Medicated Pad
  • RxCUI: 895749 - benzocaine 6 % / isopropyl alcohol 60 % Topical Swab

Clinical Specifications

Proprietary Name
Aid And First Sting Relief Prep Pad
Dosage Form
-
Usage Information
Adults and children 2 years of age and older use on hands and face to clean and refresh, allow skin to air dryFor children under 2 years ask a doctor before use.Tear open packet, unfold towelltte and use to clean desired skin area, discard towelltte appropriately after use.

Regulatory & Marketing

Labeler Name
Yiwu Haoding Medical Co.,ltd
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-09-2024
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 69139-203-01 identifies a specific commercial package of 1 packet in 1 package / .3 g in 1 packet of Aid And First Sting Relief Prep Pad, labeled by Yiwu Haoding Medical 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 Yiwu Haoding Medical Co.,ltd on January 09, 2024. The current certification is valid through December 31, 2025.

How is this Yiwu Haoding Medical Co.,ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69139020301. 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)
69139-203-01
11-Digit CMS (5-4-2)
69139-0203-01

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