Nozin Nasal Sanitizer (antiseptic) Liquid
NDC Package 82539-211-11

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Nozin Nasal Sanitizer (antiseptic) (alcohol) liquids is wipe nostrils with tissue shake ampule well for 5 seconds remove ampule, flip and reinsert into sleeve to expose swab tip. This formulation utilizes a liquid delivery system. Marketed by Global Life Technologies Corp., this product is identified by NDC 82539-211 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
82539-211-11
Package Description
100 BLISTER PACK in 1 CASE / 2 AMPULE in 1 BLISTER PACK / .6 mL in 1 AMPULE
Product Code
11-Digit Billing Format
82539021111

Clinical Specifications

Proprietary Name
Nozin Nasal Sanitizer (antiseptic)
Non-Proprietary Name
Alcohol
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
Nasal - Administration to the nose; administered by way of the nose.
Active Ingredient(s)
Usage Information
Wipe nostrils with tissue shake ampule well for 5 seconds remove ampule, flip and reinsert into sleeve to expose swab tip. Avoid touching swab tip. at dot on sleeve, squeeze firmly to crack inner ampule. point swab tip down, squeeze sleeve repeatedly to saturate swab tip Application steps: 1. Insert swab tip into RIGHT nostril. Do not go deeper than tip of swab. 2. With moderate pressure, swab around nostril eight (8) times clockwise. Cover all surfaces including inside tip of nostril. 3. squeeze to resaturate swab tip 4. insert ampule into RIGHT nostril again and swab eight (8) times counterclockwise 5. repeat steps 1, 2, 3, 4 in LEFT nostril 6. discard used ampule repeat all directions with second ampule, but skip tissue step.

Regulatory & Marketing

Labeler Name
Global Life Technologies Corp.
Product Type
Human Otc Drug
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-01-2006
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (82539-211). Click a package code to view its specific billing and regulatory data.

2 BOX in 1 CASE / 250 AMPULE in 1 BOX / .6 mL in 1 AMPULE
250 BLISTER PACK in 1 CASE / 1 AMPULE in 1 BLISTER PACK / .6 mL in 1 AMPULE
2 BOX in 1 CASE / 200 BLISTER PACK in 1 BOX / 1 AMPULE in 1 BLISTER PACK / .6 mL in 1 AMPULE
150 POUCH in 1 CASE / 1 AMPULE in 1 POUCH / .82 mL in 1 AMPULE

* 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 82539-211-11 identifies a specific commercial package of 100 blister pack in 1 case / 2 ampule in 1 blister pack / .6 ml in 1 ampule of Nozin Nasal Sanitizer (antiseptic), a human over the counter drug labeled by Global Life Technologies Corp.. This liquid is formulated for nasal 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 Global Life Technologies Corp. on January 01, 2006. The current certification is valid through December 31, 2026.

How is this Global Life Technologies Corp. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82539021111. 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)
82539-211-11
11-Digit CMS (5-4-2)
82539-0211-11

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