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NDC 62032-538 Obagi Nu-derm Fx System Normal - Oily Skin Transformation Complexion Brightening System

Homosalate,Octisalate,And Zinc Oxide Kit - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 62032-538?
  5. Obagi Nu-derm Fx System Normal - Oily Skin Transformation Complexion Brightening System Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
62032-538
Proprietary Name:
Obagi Nu-derm Fx System Normal - Oily Skin Transformation Complexion Brightening System
Non-Proprietary Name: [1]
Homosalate, Octisalate, And Zinc Oxide
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Obagi Cosmeceuticals Llc
Labeler Code:
62032
Product Label ID:
04cec275-161a-41d2-b171-33d11f15d324
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date: [9]
12-02-2019
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
BLUE (C48333)
WHITE (C48325)

Product Packages

NDC Code 62032-538-91

Package Description: 1 KIT in 1 CARTON * 198 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 48 g in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC * 85 g in 1 TUBE * 57 g in 1 BOTTLE, PLASTIC

Product Details

What is NDC 62032-538?

The NDC code 62032-538 is assigned by the FDA to the product Obagi Nu-derm Fx System Normal - Oily Skin Transformation Complexion Brightening System which is a human over the counter drug product labeled by Obagi Cosmeceuticals Llc. The generic name of Obagi Nu-derm Fx System Normal - Oily Skin Transformation Complexion Brightening System is homosalate, octisalate, and zinc oxide. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 62032-538-91 1 kit in 1 carton * 198 ml in 1 bottle, plastic * 57 g in 1 bottle, plastic * 57 g in 1 bottle, plastic * 48 g in 1 bottle, plastic * 198 ml in 1 bottle, plastic * 85 g in 1 tube * 57 g in 1 bottle, plastic. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Obagi Nu-derm Fx System Normal - Oily Skin Transformation Complexion Brightening System?

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

Which are Obagi Nu-derm Fx System Normal - Oily Skin Transformation Complexion Brightening System UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Obagi Nu-derm Fx System Normal - Oily Skin Transformation Complexion Brightening System Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".