Blippi Hand Sanitizer
NDC Package 70108-059-01

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.

Blippi Hand Sanitizer is put a thumbnail size amount in your palm and rub your hands together briskly until dry. Marketed by Ashtel Studios, Inc, this product is identified by NDC 70108-059 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
70108-059-01
Package Description
29 mL in 1 BOTTLE
Product Code
70108-059
11-Digit Billing Format
70108005901
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Blippi Hand Sanitizer
Dosage Form
-
Usage Information
Put a thumbnail size amount in your palm and rub your hands together briskly until dry. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

Regulatory & Marketing

Labeler Name
Ashtel Studios, Inc
FDA Application #
part333A
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
06-17-2020
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 70108-059-01 identifies a specific commercial package of 29 ml in 1 bottle of Blippi Hand Sanitizer, labeled by Ashtel Studios, 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 Ashtel Studios, Inc on June 17, 2020. The current certification is valid through December 31, 2023.

How is this Ashtel Studios, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70108005901. 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)
70108-059-01
11-Digit CMS (5-4-2)
70108-0059-01

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