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  4. NDC Product Code: 62839-0125 Nu Skin 180 Degree Uv Block Hydrator Spf 18

NDC 62839-0125 Nu Skin 180 Degree Uv Block Hydrator Spf 18

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62839-0125?
  4. Nu Skin 180 Degree Uv Block Hydrator Spf 18 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:
62839-0125
Proprietary Name:
Nu Skin 180 Degree Uv Block Hydrator Spf 18
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nse Products, Inc.
Labeler Code:
62839
Product Label ID:
b9635e59-bb08-4167-b7ba-54c3fc712589
Start Marketing Date: [9]
06-10-2001
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 62839-0125?

The NDC code 62839-0125 is assigned by the FDA to the product Nu Skin 180 Degree Uv Block Hydrator Spf 18 which is product labeled by Nse Products, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62839-0125-4 1 bottle, pump in 1 carton / 30 ml in 1 bottle, pump. 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 Skin 180 Degree Uv Block Hydrator Spf 18?

Use in the morning as the fourth step in the Nu Skin 180°® System. Apply lightly in an upward, outward motion to face and neck, avoiding the eye area.

Which are Nu Skin 180 Degree Uv Block Hydrator Spf 18 UNII Codes?

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

Which are Nu Skin 180 Degree Uv Block Hydrator Spf 18 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

[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".