Purehold Antiseptic Instant Hand Sanitizer Gel
NDC Package 70079-101-01

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

Package Information

Purehold Antiseptic Instant Hand Sanitizer (ethyl alcohol, isopropyl alcohol) gel is use Hand sanitizer to help reduce bacteria on the skin. This formulation utilizes a gel delivery system. Marketed by Pure Hold Ltd, this product is identified by NDC 70079-101 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
70079-101-01
Package Description
850 mL in 1 BOTTLE
Product Code
70079-101
11-Digit Billing Format
70079010101
RxNorm Crosswalk
  • RxCUI: 1666879 - ethanol 75 % / isopropyl alcohol 4 % Topical Gel
  • RxCUI: 1666879 - ethanol 0.75 ML/ML / isopropyl alcohol 0.04 ML/ML Topical Gel

Clinical Specifications

Proprietary Name
Purehold Antiseptic Instant Hand Sanitizer
Non-Proprietary Name
Ethyl Alcohol, Isopropyl Alcohol
Substance Name
Alcohol; Isopropyl Alcohol
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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)
Usage Information
Use Hand sanitizer to help reduce bacteria on the skin

Regulatory & Marketing

Labeler Name
Pure Hold Ltd
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-03-2015
End Marketing Date
08-31-2027
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 70079-101-01 identifies a specific commercial package of 850 ml in 1 bottle of Purehold Antiseptic Instant Hand Sanitizer, a human over the counter drug labeled by Pure Hold Ltd. This gel is formulated for topical use and contains alcohol; isopropyl alcohol 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 Pure Hold Ltd on August 03, 2015.

How is this Pure Hold Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70079010101. 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)
70079-101-01
11-Digit CMS (5-4-2)
70079-0101-01

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