1. Home
  2. Labeler Index
  3. Omp, Inc.
  4. NDC Product Code: 62032-527 Obagi Nu-derm Fx System - Normal To Dry

NDC 62032-527 Obagi Nu-derm Fx System - Normal To Dry

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62032-527?
  4. Obagi Nu-derm Fx System - Normal To Dry Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
62032-527
Proprietary Name:
Obagi Nu-derm Fx System - Normal To Dry
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Omp, Inc.
Labeler Code:
62032
Product Label ID:
50dcfca5-cb2d-452d-a5e9-050d6561b567
Start Marketing Date: [9]
11-04-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 62032-527?

The NDC code 62032-527 is assigned by the FDA to the product Obagi Nu-derm Fx System - Normal To Dry which is product labeled by Omp, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62032-527-07 1 kit in 1 carton * 85 g in 1 tube. 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 To Dry?

Use twice daily, morning and evening. Massage a small amount of cleanser and water onto skin. Rinse with lukewarm water and gently pat dry. Use daily, in the morning and evening after cleansing. Shake before use. Saturate a cotton pad and gently wipe over the entire face. Do not rinse. Use daily, in the morning and evening. Squeeze a small amount (approximately 1 to 2 pea-size drops) onto your hand. Apply evenly to the entire face, extending to the hairline, over the ears, and ending with a feathering motion, or as directed by your physician. Use daily, in the morning. Squeeze a small amount (approximately 1 to 2 pea-size drops) onto your hands. Using your fingertips, apply evenly to the entire face. Massage until completely absorbed. Apply to face in the morning and evening or as needed. Use daily in the evening. Squeeze a small amount (approximately 1 to 2 pea-size drops onto your hand. Apply evenly to the entire face, extending to the hairline, over the ears, and ending with a feathering motion, or as directed by your physician. •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

Which are Obagi Nu-derm Fx System - Normal To Dry UNII Codes?

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

Which are Obagi Nu-derm Fx System - Normal To Dry 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:

* Please review the disclaimer below.

Product Footnotes

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

[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".