Alcohol Prep Pads With Pain Relief
NDC Package 49348-897-39

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.

Alcohol Prep Pads With Pain Relief is prior to Injection - Adults and children 2 years of age or older:Apply to the skin just prior to injection. Marketed by Mckesson, this product is identified by NDC 49348-897 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
49348-897-39
Package Description
80 PACKET in 1 CARTON / 1 SWAB in 1 PACKET
Product Code
49348-897
11-Digit Billing Format
49348089739
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
80 EA
RxNorm Crosswalk
  • RxCUI: 809206 - benzocaine 6 % / isopropyl alcohol 70 % Medicated Pad
  • RxCUI: 809206 - benzocaine 60 MG/ML / isopropyl alcohol 0.7 ML/ML Medicated Pad
  • RxCUI: 809206 - benzocaine 6 % / isopropyl alcohol 70 % Topical Swab

Clinical Specifications

Proprietary Name
Alcohol Prep Pads With Pain Relief
Dosage Form
-
Usage Information
Prior to Injection - Adults and children 2 years of age or older:Apply to the skin just prior to injection. Benzocaine takes a minute to act. for best results, wait briefly and then make injection.Insect bites, skin irritations, minor burns, sunburn - Adults and children 2 years of age or older:Apply to the affected site not more than 3 to 4 times daily.Children under 2 years of age: Ask a doctor.

Regulatory & Marketing

Labeler Name
Mckesson
FDA Application #
part348
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
02-19-2010
Listing Expiration
12-31-2017
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 49348-897-39 identifies a specific commercial package of 80 packet in 1 carton / 1 swab in 1 packet of Alcohol Prep Pads With Pain Relief, labeled by Mckesson. This product is billed for "EA" each discreet unit and contains an estimated amount of 80 billable units per package. 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 Mckesson on February 19, 2010. The current certification is valid through December 31, 2017.

How is this Mckesson product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49348089739. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 80 total billable units per package. 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)
49348-897-39
11-Digit CMS (5-4-2)
49348-0897-39

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