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  5. NDC Package Code: 62296-8292-2 Ulta Face Spf 30

NDC Package 62296-8292-2 Ulta Face Spf 30

Avobenzone,Homosalate,Octisalate,Octocrylene,Oxybenzone Lotion 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:
62296-8292-2
Package Description:
88 g in 1 BOTTLE
Product Code:
62296-8292
Proprietary Name:
Ulta Face Spf 30
Non-Proprietary Name:
Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Substance Name:
Avobenzone; Homosalate; Octisalate; Octocrylene; Oxybenzone
Usage Information:
Apply liberally 15 minutes before sun exposurereapply: after 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hoursSun 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 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-sleeve shirts, pants, hats, and sunglasseschildren under 6 months of age: Ask a doctor
11-Digit NDC Billing Format:
62296829202
Product Type:
Human Otc Drug
Labeler Name:
Ulta
Dosage Form:
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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:
part352
Marketing Category:
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date:
08-17-2015
Listing Expiration Date:
12-31-2025
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 62296-8292-2?

The NDC Packaged Code 62296-8292-2 is assigned to a package of 88 g in 1 bottle of Ulta Face Spf 30, a human over the counter drug labeled by Ulta. The product's dosage form is lotion and is administered via topical form.

Is NDC 62296-8292 included in the NDC Directory?

Yes, Ulta Face Spf 30 with product code 62296-8292 is active and included in the NDC Directory. The product was first marketed by Ulta on August 17, 2015 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 62296-8292-2?

The 11-digit format is 62296829202. 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 5-4-1 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
5-4-162296-8292-25-4-262296-8292-02