Nunature First Aid Gel
NDC Package 51879-211-01

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Nunature First Aid Gel is uses ​​​First aid to help prevent infection in minor: cuts scrapesburns For the temporary relief of pain or discomfort in minor:cutsscrapesburns. Marketed by Tec Laboratories Inc, this product is identified by NDC 51879-211 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
51879-211-01
Package Description
28.3 g in 1 TUBE
Product Code
51879-211
11-Digit Billing Format
51879021101

Clinical Specifications

Proprietary Name
Nunature First Aid Gel
Dosage Form
-
Usage Information
Uses ​​​First aid to help prevent infection in minor: cuts scrapesburns For the temporary relief of pain or discomfort in minor:cutsscrapesburns

Regulatory & Marketing

Labeler Name
Tec Laboratories Inc
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-11-2022
End Marketing Date
05-31-2026
Listing Expiration
05-31-2026
Exclude Flag
D
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 51879-211-01 identifies a specific commercial package of 28.3 g in 1 tube of Nunature First Aid Gel, labeled by Tec Laboratories Inc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Tec Laboratories Inc on August 11, 2022. The current certification is valid through May 31, 2026.

How is this Tec Laboratories Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51879021101. 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)
51879-211-01
11-Digit CMS (5-4-2)
51879-0211-01

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