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  4. NDC Product Code: 62032-104 Nu-derm Sun Shield Broad Spectrum Spf 50 Matte Sunscreen

NDC 62032-104 Nu-derm Sun Shield Broad Spectrum Spf 50 Matte Sunscreen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62032-104?
  4. Nu-derm Sun Shield Broad Spectrum Spf 50 Matte Sunscreen Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
62032-104
Proprietary Name:
Nu-derm Sun Shield Broad Spectrum Spf 50 Matte Sunscreen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Omp, Inc.
Labeler Code:
62032
Product Label ID:
7e70faa2-ce6a-4815-9fa1-43c7025d80e6
Start Marketing Date: [9]
11-07-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 62032-104-10

Package Description: 28 g in 1 TUBE

NDC Code 62032-104-90

Package Description: 85 g in 1 TUBE

Product Details

What is NDC 62032-104?

The NDC code 62032-104 is assigned by the FDA to the product Nu-derm Sun Shield Broad Spectrum Spf 50 Matte Sunscreen which is product labeled by Omp, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 62032-104-10 28 g in 1 tube , 62032-104-90 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 Nu-derm Sun Shield Broad Spectrum Spf 50 Matte Sunscreen?

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. Saturate a cotton pad and gently wipe over entire face. Do not rinse. Use daily, in the morning. Squeeze a small amount (approximately 1-2 pea-sized 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. apply liberally 15 minutes before sun exposureuse a water resistant sunscreen if swimming or sweatingreapply at least every 2 hourschildren under 6 months: Ask a doctorSun 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 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 Nu-derm Sun Shield Broad Spectrum Spf 50 Matte Sunscreen UNII Codes?

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

Which are Nu-derm Sun Shield Broad Spectrum Spf 50 Matte Sunscreen 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:

What is the NDC to RxNorm Crosswalk for Nu-derm Sun Shield Broad Spectrum Spf 50 Matte Sunscreen?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".