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  5. NDC Package Code: 85313-211-04 Non-tinted Mineral Foaming Sunscreen

NDC Package 85313-211-04 Non-tinted Mineral Foaming Sunscreen

Titanium Dioxide,Zinc Oxide Aerosol, Foam 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:
85313-211-04
Package Description:
113 g in 1 BOTTLE, PUMP
Product Code:
85313-211
Proprietary Name:
Non-tinted Mineral Foaming Sunscreen
Non-Proprietary Name:
Titanium Dioxide, Zinc Oxide
Substance Name:
Titanium Dioxide; Zinc Oxide
11-Digit NDC Billing Format:
85313021104
Product Type:
Human Otc Drug
Labeler Name:
Restore Skin Therapy, Llc
Dosage Form:
Aerosol, Foam - A dosage form containing one or more active ingredients, surfactants, aqueous or nonaqueous liquids, and the propellants; if the propellant is in the internal (discontinuous) phase (i.e., of the oil-in-water type), a stable foam is discharged, and if the propellant is in the external (continuous) phase (i.e., of the water-in-oil type), a spray or a quick-breaking foam is discharged.
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:
08-05-2019
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 85313-211-04?

The NDC Packaged Code 85313-211-04 is assigned to a package of 113 g in 1 bottle, pump of Non-tinted Mineral Foaming Sunscreen, a human over the counter drug labeled by Restore Skin Therapy, Llc. The product's dosage form is aerosol, foam and is administered via topical form.

Is NDC 85313-211 included in the NDC Directory?

Yes, Non-tinted Mineral Foaming Sunscreen with product code 85313-211 is active and included in the NDC Directory. The product was first marketed by Restore Skin Therapy, Llc on August 05, 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 85313-211-04?

The 11-digit format is 85313021104. 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
5-3-285313-211-045-4-285313-0211-04