Povidone-iodine Prep Pads Medium Cloth
NDC Package 51662-1667-1

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

Package Information

Povidone-iodine Prep Pads Medium cloths is clean the affected area apply a small amount of this product on the area 1 to 3 times daily. This formulation utilizes a cloth delivery system. Marketed by Hf Acquisition Co. Llc, Dba Healthfirst, this product is identified by NDC 51662-1667 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
51662-1667-1
Package Description
2 PACKET in 1 PACKET / 1 mL in 1 PACKET
Product Code
51662-1667
11-Digit Billing Format
51662166701
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Povidone-iodine Prep Pads Medium
Non-Proprietary Name
Povidone-iodine Prep Pads Medium
Substance Name
Povidone-iodine
Dosage Form
Cloth - A large piece of relatively flat, absorbent material that contains a drug. It 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
Clean the affected area apply a small amount of this product on the area 1 to 3 times daily. may be covered with a sterile bandage if bandaged, let dry first

Regulatory & Marketing

Labeler Name
Hf Acquisition Co. Llc, Dba Healthfirst
Product Type
Human Otc Drug
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-01-2007
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 51662-1667-1 identifies a specific commercial package of 2 packet in 1 packet / 1 ml in 1 packet of Povidone-iodine Prep Pads Medium, a human over the counter drug labeled by Hf Acquisition Co. Llc, Dba Healthfirst. This cloth 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 Hf Acquisition Co. Llc, Dba Healthfirst on January 01, 2007. The current certification is valid through December 31, 2026.

How is this Hf Acquisition Co. Llc, Dba Healthfirst product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51662166701. 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)
51662-1667-1
11-Digit CMS (5-4-2)
51662-1667-01

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