Lola Vaginal Itch Relief Wipes
NDC Package 81032-422-28

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.

Lola Vaginal Itch Relief Wipes is adults and children 12 years and older. Marketed by Alyk, Inc., this product is identified by NDC 81032-422 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
81032-422-28
Package Description
28 CLOTH in 1 POUCH
Product Code
81032-422
11-Digit Billing Format
81032042228
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Lola Vaginal Itch Relief Wipes
Dosage Form
-
Usage Information
Adults and children 12 years and older. Unfold towelette and gently wipe external vaginal area. Use each towelette only once and then throw away. Use no more than 3 to 4 times daily.

Regulatory & Marketing

Labeler Name
Alyk, Inc.
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
03-31-2021
Listing Expiration
12-31-2023
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 81032-422-28 identifies a specific commercial package of 28 cloth in 1 pouch of Lola Vaginal Itch Relief Wipes, labeled by Alyk, Inc.. 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 Alyk, Inc. on March 31, 2021. The current certification is valid through December 31, 2023.

How is this Alyk, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 81032042228. 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)
81032-422-28
11-Digit CMS (5-4-2)
81032-0422-28

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