Gin-iii Alpha And Omega Gin Sun
NDC Package 71135-100-02

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 inactivated by the FDA.

Gin-iii Alpha And Omega Gin Sun is apply the adequate amount on the palm of the hands and pat lightly with the fingertips.• Apply liberally 15 minutes before sun exposure.• Reapply at least every 2 hours.• Use a water-resistant sunscreen if swimming or sweating.• Sun Protection Measures. Marketed by Hanwool Life Sciences. Co., Ltd, this product is identified by NDC 71135-100 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
71135-100-02
Package Description
1 TUBE in 1 PACKAGE / 50 mL in 1 TUBE (71135-100-01)
Product Code
71135-100
11-Digit Billing Format
71135010002

Clinical Specifications

Proprietary Name
Gin-iii Alpha And Omega Gin Sun
Dosage Form
-
Usage Information
Apply the adequate amount on the palm of the hands and pat lightly with the fingertips.• Apply liberally 15 minutes before sun exposure.• Reapply at least every 2 hours.• Use a water-resistant sunscreen if swimming or sweating.• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m. - 2 p.m. Wear long-sleeved shirts, pants, hats, and sunglasses.• Children under 6 months of age: ask a doctor

Regulatory & Marketing

Labeler Name
Hanwool Life Sciences. Co., Ltd
FDA Application #
part352
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
12-12-2016
Listing Expiration
12-31-2018
Exclude Flag
I
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 71135-100-02 identifies a specific commercial package of 1 tube in 1 package / 50 ml in 1 tube (71135-100-01) of Gin-iii Alpha And Omega Gin Sun, labeled by Hanwool Life Sciences. Co., Ltd. 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 Hanwool Life Sciences. Co., Ltd on December 12, 2016. The current certification is valid through December 31, 2018.

How is this Hanwool Life Sciences. Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71135010002. 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)
71135-100-02
11-Digit CMS (5-4-2)
71135-0100-02

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