Aniosgel 85 Gel
NDC Package 62169-203-12

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

Package Information

Aniosgel 85 (ethanol) gel is • A hand rub to decrease bacteria on the skin. This formulation utilizes a gel delivery system. Marketed by Laboratoires Anios, this product is identified by NDC 62169-203 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
62169-203-12
Package Description
12 BOTTLE, PLASTIC in 1 PACKAGE / 500 mL in 1 BOTTLE, PLASTIC (62169-203-17)
Product Code
62169-203
11-Digit Billing Format
62169020312

Clinical Specifications

Proprietary Name
Aniosgel 85 Npc
Non-Proprietary Name
Ethanol
Substance Name
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)
ALCOHOL 377.5 mL/500mL
Usage Information
• A hand rub to decrease bacteria on the skin.

Regulatory & Marketing

Labeler Name
Laboratoires Anios
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-01-2014
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 62169-203-12 identifies a specific commercial package of 12 bottle, plastic in 1 package / 500 ml in 1 bottle, plastic (62169-203-17) of Aniosgel 85 Npc, a human over the counter drug labeled by Laboratoires Anios. This gel 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 Laboratoires Anios on April 01, 2014.

How is this Laboratoires Anios product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 62169020312. 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)
62169-203-12
11-Digit CMS (5-4-2)
62169-0203-12

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