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  5. NDC Package Code: 62032-539-07 Obagi Nu-derm Fx System Normal - Dry Skin Transformation Complexion Brightening System

NDC Package 62032-539-07 Obagi Nu-derm Fx System Normal - Dry Skin Transformation Complexion Brightening System

Homosalate,Octisalate,And Zinc Oxide Kit - 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:
62032-539-07
Package Description:
1 KIT in 1 CARTON * 48 g in 1 BOTTLE, PLASTIC * 85 g in 1 TUBE * 57 g in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC
Product Code:
62032-539
Proprietary Name:
Obagi Nu-derm Fx System Normal - Dry Skin Transformation Complexion Brightening System
Non-Proprietary Name:
Homosalate, Octisalate, And Zinc Oxide
Usage Information:
Apply liberally 15 minutes before sun exposureuse a water resistant sunscreen if swimming or sweatingreapply at 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 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 sunglasseschildren under 6 months: Ask a doctor
11-Digit NDC Billing Format:
62032053907
Product Type:
Human Otc Drug
Labeler Name:
Obagi Cosmeceuticals Llc
Dosage Form:
Kit - A packaged collection of related material.
Sample Package:
No
Marketing Category:
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date:
12-02-2019
Listing Expiration Date:
12-31-2024
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 62032-539-07?

The NDC Packaged Code 62032-539-07 is assigned to a package of 1 kit in 1 carton * 48 g in 1 bottle, plastic * 85 g in 1 tube * 57 g in 1 bottle, plastic * 198 ml in 1 bottle, plastic * 57 g in 1 bottle, plastic * 57 g in 1 bottle, plastic * 198 ml in 1 bottle, plastic of Obagi Nu-derm Fx System Normal - Dry Skin Transformation Complexion Brightening System, a human over the counter drug labeled by Obagi Cosmeceuticals Llc. The product's dosage form is kit and is administered via form.

Is NDC 62032-539 included in the NDC Directory?

Yes, Obagi Nu-derm Fx System Normal - Dry Skin Transformation Complexion Brightening System with product code 62032-539 is active and included in the NDC Directory. The product was first marketed by Obagi Cosmeceuticals Llc on December 02, 2019 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 62032-539-07?

The 11-digit format is 62032053907. 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
5-3-262032-539-075-4-262032-0539-07