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  5. NDC Package Code: 62032-580-88 Obagi 360

NDC Package 62032-580-88 Obagi 360

Avobenzone,Octinoxate,Octisalate,Oxybenzone 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:
62032-580-88
Package Description:
1 KIT in 1 CARTON * 150 mL in 1 TUBE * 28 g in 1 TUBE * 75 g in 1 TUBE
Product Code:
62032-580
Proprietary Name:
Obagi 360
Non-Proprietary Name:
Avobenzone, Octinoxate, Octisalate, Oxybenzone
Usage Information:
Use twice daily, morning and evening. Wet hands and face, then massage cleanser onto skin with a gentle circular motion. Rinse with lukewarm water and gently pat dry. Once daily in the evening, apply a pearl-size amount to the face and gently smooth until absorbed. •apply liberally 15 minutes before sun exposure•use a water resistant sunscreen if swimming or sweating•reapply at least every 2 hours•children under 6 months: Ask a doctor•Sun 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 sunglasses
11-Digit NDC Billing Format:
62032058088
Product Type:
Human Otc Drug
Labeler Name:
Omp, Inc.
Dosage Form:
Kit - A packaged collection of related material.
Sample Package:
No
FDA Application Number:
part352
Marketing Category:
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date:
09-08-2015
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 62032-580-88?

The NDC Packaged Code 62032-580-88 is assigned to a package of 1 kit in 1 carton * 150 ml in 1 tube * 28 g in 1 tube * 75 g in 1 tube of Obagi 360, a human over the counter drug labeled by Omp, Inc.. The product's dosage form is kit and is administered via form.

Is NDC 62032-580 included in the NDC Directory?

Yes, Obagi 360 with product code 62032-580 is active and included in the NDC Directory. The product was first marketed by Omp, Inc. on September 08, 2015 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 62032-580-88?

The 11-digit format is 62032058088. 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
5-3-262032-580-885-4-262032-0580-88