Pvp-i Prep Pad Swab
NDC Package 10819-3801-2

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

Package Information

Pvp-i Prep Pad (povidone-iodine) swabs is tear at notchClean the treatment areaRemove swabApply to the operative site prior to surgeryAllow to dry. This formulation utilizes a swab delivery system. Marketed by Professional Disposables International, Inc., this product is identified by NDC 10819-3801 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
10819-3801-2
Package Description
100 PACKET in 1 BOX / .485 mL in 1 PACKET (10819-3801-1)
Product Code
10819-3801
11-Digit Billing Format
10819380102

Clinical Specifications

Proprietary Name
Pvp-i Prep Pad
Non-Proprietary Name
Povidone-iodine
Substance Name
Povidone-iodine
Dosage Form
Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab is typically used for applying medication or for cleansing.
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)
POVIDONE-IODINE 10 mg/mL
Usage Information
Tear at notchClean the treatment areaRemove swabApply to the operative site prior to surgeryAllow to dry

Regulatory & Marketing

Labeler Name
Professional Disposables International, Inc.
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-22-2026
Listing Expiration
12-31-2027
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 10819-3801-2 identifies a specific commercial package of 100 packet in 1 box / .485 ml in 1 packet (10819-3801-1) of Pvp-i Prep Pad, a human over the counter drug labeled by Professional Disposables International, Inc.. This swab is formulated for topical use and contains povidone-iodine 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 Professional Disposables International, Inc. on June 22, 2026. The current certification is valid through December 31, 2027.

How is this Professional Disposables International, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 10819380102. 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)
10819-3801-2
11-Digit CMS (5-4-2)
10819-3801-02

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