NDC Package 85926-202-50 Uv Protection Veil Mineral Sunscreen Non Tinted

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

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:
85926-202-50
Package Description:
53 g in 1 BOTTLE, PUMP
Product Code:
Proprietary Name:
Uv Protection Veil Mineral Sunscreen Non Tinted
Non-Proprietary Name:
Titanium Dioxide, Zinc Oxide
Substance Name:
Titanium Dioxide; Zinc Oxide
Usage Information:
Apply liberally 15 minutes before sun exposure. Use a water-resistant product if swimming or sweating. Reapply at least every 2 hours. Children under 6 months: Ask a doctor. 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.
11-Digit NDC Billing Format:
85926020250
Product Type:
Human Otc Drug
Labeler Name:
Athena Plastic Surgery
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(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.
Sample Package:
No
FDA Application Number:
M020
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
10-24-2019
Listing Expiration Date:
12-31-2026
Exclude Flag:
N

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.

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Frequently Asked Questions

What is NDC 85926-202-50?

The NDC Packaged Code 85926-202-50 is assigned to a package of 53 g in 1 bottle, pump of Uv Protection Veil Mineral Sunscreen Non Tinted, a human over the counter drug labeled by Athena Plastic Surgery. The product's dosage form is cream and is administered via topical form.

Is NDC 85926-202 included in the NDC Directory?

Yes, Uv Protection Veil Mineral Sunscreen Non Tinted with product code 85926-202 is active and included in the NDC Directory. The product was first marketed by Athena Plastic Surgery on October 24, 2019 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 85926-202-50?

The 11-digit format is 85926020250. 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
5-3-285926-202-505-4-285926-0202-50