Instant Hand Sanitizer Liquid
NDC Package 69060-6930-2

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

Package Information

Instant Hand Sanitizer liquids is place a palmful ( 5 grams) of product in one hand,.Spread on both hands and rub into the skin until dry (approximately 1 to 2 minutes).Place a smaller amount (2.5 grams) into one hand, spread over both hands to wrist and rub into the skin until dry (approximately 30 seconds).Will air dry in 15 seconds. This formulation utilizes a liquid delivery system. Marketed by Rainbow Technology Corporation, this product is identified by NDC 69060-6930 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
69060-6930-2
Package Description
236 mL in 1 BOTTLE, PLASTIC
Product Code
69060-6930
11-Digit Billing Format
69060693002

Clinical Specifications

Proprietary Name
Instant Hand Sanitizer
Non-Proprietary Name
Instant Hand Sanitizer
Substance Name
Alcohol
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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)
ALCOHOL 67 mL/100mL
Usage Information
Place a palmful ( 5 grams) of product in one hand,.Spread on both hands and rub into the skin until dry (approximately 1 to 2 minutes).Place a smaller amount (2.5 grams) into one hand, spread over both hands to wrist and rub into the skin until dry (approximately 30 seconds).Will air dry in 15 seconds.

Regulatory & Marketing

Labeler Name
Rainbow Technology Corporation
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-24-2013
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 69060-6930-2 identifies a specific commercial package of 236 ml in 1 bottle, plastic of Instant Hand Sanitizer, a human over the counter drug labeled by Rainbow Technology Corporation. This liquid is formulated for topical use and contains 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 Rainbow Technology Corporation on May 24, 2013. The current certification is valid through December 31, 2026.

How is this Rainbow Technology Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69060693002. 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)
69060-6930-2
11-Digit CMS (5-4-2)
69060-6930-02

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