Obagi Nu-derm System Normal-dry Skin Transformation Trial Kit
NDC Package 62032-913-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Obagi Nu-derm System Normal-dry Skin Transformation Trial (hydroquinone, homosalate, octisalate, zinc oxide) kits is apply liberally 15 minutes before sun exposureuse a water resistant sunscreen if swimming or sweatingreapply at least every 2 hoursSun Protection Measures. This formulation utilizes a kit delivery system. Marketed by Obagi Cosmeceuticals Llc, this product is identified by NDC 62032-913.

Identification & Billing

NDC Package Code
62032-913-01
Package Description
1 KIT in 1 CARTON * 28 g in 1 BOTTLE, PLASTIC * 59 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-100-36) * 28 g in 1 TUBE (62032-140-05) * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 59 mL in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
62032091301
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Obagi Nu-derm System Normal-dry Skin Transformation Trial
Non-Proprietary Name
Hydroquinone, Homosalate, Octisalate, Zinc Oxide
Dosage Form
Kit - A packaged collection of related material.
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

Regulatory & Marketing

Labeler Name
Obagi Cosmeceuticals Llc
Product Type
Human Otc Drug
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
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 62032-913-01 identifies a specific commercial package of 1 kit in 1 carton * 28 g in 1 bottle, plastic * 59 ml in 1 bottle, plastic * 57 g in 1 bottle, plastic (62032-100-36) * 28 g in 1 tube (62032-140-05) * 57 g in 1 bottle, plastic (62032-101-36) * 59 ml in 1 bottle, plastic of Obagi Nu-derm System Normal-dry Skin Transformation Trial, a human over the counter drug labeled by Obagi Cosmeceuticals Llc. This kit is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Obagi Cosmeceuticals Llc on December 02, 2019. The current certification is valid through December 31, 2026.

How is this Obagi Cosmeceuticals Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 62032091301. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
62032-913-01
11-Digit CMS (5-4-2)
62032-0913-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.