Water-based Personal Lubricant, Acvioo 001
NDC Package 71847-2215-5

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Water-based Personal Lubricant, Acvioo 001 is aCVIOO 001 is a water-based personal lubricant, for penile and/or vaginal application, intended to lubricate and moisturize, to enhance the ease and comfort of intimate sexual activity, help relieve virginal dryness, and supplement to the body's natural lubricant.Apply a small amount to genital areas. Marketed by Shenzhen Dikailong Technology Ltd, this product is identified by NDC 71847-2215.

Identification & Billing

NDC Package Code
71847-2215-5
Package Description
240 mL in 1 BOTTLE
Product Code
71847-2215
11-Digit Billing Format
71847221505

Clinical Specifications

Proprietary Name
Water-based Personal Lubricant, Acvioo 001
Dosage Form
-
Usage Information
ACVIOO 001 is a water-based personal lubricant, for penile and/or vaginal application, intended to lubricate and moisturize, to enhance the ease and comfort of intimate sexual activity, help relieve virginal dryness, and supplement to the body's natural lubricant.Apply a small amount to genital areas. Reapply as needed or desired.

Regulatory & Marketing

Labeler Name
Shenzhen Dikailong Technology Ltd
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
10-30-2017
Listing Expiration
12-31-2020
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (71847-2215). Click a package code to view its specific billing and regulatory data.

71847-2215-7
400 mL in 1 BOTTLE

* 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 71847-2215-5 identifies a specific commercial package of 240 ml in 1 bottle of Water-based Personal Lubricant, Acvioo 001, labeled by Shenzhen Dikailong Technology 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 Shenzhen Dikailong Technology Ltd on October 30, 2017. The current certification is valid through December 31, 2020.

How is this Shenzhen Dikailong Technology Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71847221505. 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)
71847-2215-5
11-Digit CMS (5-4-2)
71847-2215-05

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