Renewaluxe Spf 50 Sunscreen Cream
NDC Package 83447-005-01

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

Package Information

Renewaluxe Spf 50 Sunscreen cream is a medication used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). This formulation utilizes a cream delivery system. Marketed by Guangzhou Fantesy Biotechnology Co.,ltd, this product is identified by NDC 83447-005 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
83447-005-01
Package Description
50 mL in 1 BOX
Product Code
83447-005
11-Digit Billing Format
83447000501

Clinical Specifications

Proprietary Name
Renewaluxe Spf 50 Sunscreen
Non-Proprietary Name
Renewaluxe Spf 50 Sunscreen
Substance Name
Zinc Oxide
Dosage Form
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route
Cutaneous - Administration to the skin.
Active Ingredient(s)
ZINC OXIDE 21.8 g/100mL
Usage Information
This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.

Regulatory & Marketing

Labeler Name
Guangzhou Fantesy Biotechnology Co.,ltd
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-26-2024
Listing Expiration
12-31-2027
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 83447-005-01 identifies a specific commercial package of 50 ml in 1 box of Renewaluxe Spf 50 Sunscreen, a human over the counter drug labeled by Guangzhou Fantesy Biotechnology Co.,ltd. This cream is formulated for cutaneous use and contains zinc oxide 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 Guangzhou Fantesy Biotechnology Co.,ltd on June 26, 2024. The current certification is valid through December 31, 2027.

What are the primary indications for this medication?

This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.

How is this Guangzhou Fantesy Biotechnology Co.,ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83447000501. 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)
83447-005-01
11-Digit CMS (5-4-2)
83447-0005-01

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