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  5. NDC Package Code: 85302-208-50 Illuminating Daily Spf 40 Lightly Tinted

NDC Package 85302-208-50 Illuminating Daily Spf 40 Lightly Tinted

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
85302-208-50
Package Description:
50 g in 1 BOTTLE, PUMP
Product Code:
85302-208
Proprietary Name:
Illuminating Daily Spf 40 Lightly Tinted
Non-Proprietary Name:
Zinc Oxide
Substance Name:
Zinc Oxide
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.
11-Digit NDC Billing Format:
85302020850
Product Type:
Human Otc Drug
Labeler Name:
Face 5, Llc
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.
  • 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:
04-17-2024
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
85302-208-151.5 g in 1 PACKET

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 85302-208-50?

The NDC Packaged Code 85302-208-50 is assigned to a package of 50 g in 1 bottle, pump of Illuminating Daily Spf 40 Lightly Tinted, a human over the counter drug labeled by Face 5, Llc. The product's dosage form is cream and is administered via topical form.

Is NDC 85302-208 included in the NDC Directory?

Yes, Illuminating Daily Spf 40 Lightly Tinted with product code 85302-208 is active and included in the NDC Directory. The product was first marketed by Face 5, Llc on April 17, 2024 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 85302-208-50?

The 11-digit format is 85302020850. 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
5-3-285302-208-505-4-285302-0208-50