Aquasource Hand Sanitizer
NDC Package 86050-4750-2

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 discontinued by the firm.

Aquasource Hand Sanitizer is a . Marketed by Blendpack, Inc., this product is identified by NDC 86050-4750 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
86050-4750-2
Package Description
208.2 L in 1 DRUM
Product Code
86050-4750
11-Digit Billing Format
86050475002

Clinical Specifications

Proprietary Name
Aquasource Hand Sanitizer
Dosage Form
-

Regulatory & Marketing

Labeler Name
Blendpack, Inc.
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-31-2024
End Marketing Date
11-05-2024
Listing Expiration
11-05-2024
Exclude Flag
D
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 (86050-4750). Click a package code to view its specific billing and regulatory data.

86050-4750-1
3.79 L in 1 JUG
86050-4750-3
1041 L in 1 TANK

* 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 86050-4750-2 identifies a specific commercial package of 208.2 l in 1 drum of Aquasource Hand Sanitizer, labeled by Blendpack, 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 Blendpack, Inc. on July 31, 2024. The current certification is valid through November 05, 2024.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 86050475002. 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)
86050-4750-2
11-Digit CMS (5-4-2)
86050-4750-02

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