Suede Hand Sanitizer Spray
NDC Package 85782-005-01

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

Package Information

Suede Hand Sanitizer (isopropyl alcohol) sprays is a human otc drug administered via topical route. This formulation utilizes a spray delivery system. Marketed by Handetizer, Llc., this product is identified by NDC 85782-005 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
85782-005-01
Package Description
20 mL in 1 BOTTLE, SPRAY
Product Code
85782-005
11-Digit Billing Format
85782000501
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Suede Hand Sanitizer
Non-Proprietary Name
Isopropyl Alcohol
Substance Name
Isopropyl Alcohol
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
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)
ISOPROPYL ALCOHOL 72 mL/100mL

Regulatory & Marketing

Labeler Name
Handetizer, Llc.
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-17-2025
Listing Expiration
12-31-2026
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 85782-005-01 identifies a specific commercial package of 20 ml in 1 bottle, spray of Suede Hand Sanitizer, a human over the counter drug labeled by Handetizer, Llc.. This spray is formulated for topical use and contains 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 Handetizer, Llc. on August 17, 2025. The current certification is valid through December 31, 2026.

How is this Handetizer, Llc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85782000501. 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)
85782-005-01
11-Digit CMS (5-4-2)
85782-0005-01

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