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  5. NDC Package Code: 85950-002-01 Yonhisdat Sunscreen Powder

NDC Package 85950-002-01 Yonhisdat Sunscreen Powder

Titanium Dioxide,Zinc Oxide Powder Powder Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
85950-002-01
Package Description:
5 g in 1 BOTTLE
Product Code:
85950-002
Proprietary Name:
Yonhisdat Sunscreen Powder
Non-Proprietary Name:
Titanium Dioxide, Zinc Oxide Powder
Substance Name:
Titanium Dioxide; Zinc Oxide
Usage Information:
Apoly liberally i5 mnutes before sunexoosure.pants, hats andsunglasses. Children under 6months of age: ask a doctor Reapph: Aler 80 minues oswinming or sneaing immetlaletater ionel dning Atleast eveny2hours.Sun precion leasures Spending ime in the sun increasesyour isk oifshincancer and eaty skinaging T decrease this rsk requlanuse a sunsren uith a bradspecnum spf value of 15 or higtherAnd ohersun prolecion measureshclud ng imtime ihthe sun especdaly fom 10am.2am.
11-Digit NDC Billing Format:
85950000201
Product Type:
Human Otc Drug
Labeler Name:
Panergytek Usa Inc
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Administration Route(s):
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):
Sample Package:
No
FDA Application Number:
M020
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
07-27-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 85950-002-01?

The NDC Packaged Code 85950-002-01 is assigned to a package of 5 g in 1 bottle of Yonhisdat Sunscreen Powder, a human over the counter drug labeled by Panergytek Usa Inc. The product's dosage form is powder and is administered via topical form.

Is NDC 85950-002 included in the NDC Directory?

Yes, Yonhisdat Sunscreen Powder with product code 85950-002 is active and included in the NDC Directory. The product was first marketed by Panergytek Usa Inc on July 27, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 85950-002-01?

The 11-digit format is 85950000201. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-285950-002-015-4-285950-0002-01