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  4. NDC Product Code: 62839-1133 Sunright Bodyblock Spf15

NDC 62839-1133 Sunright Bodyblock Spf15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62839-1133?
  4. Sunright Bodyblock Spf15 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:
62839-1133
Proprietary Name:
Sunright Bodyblock Spf15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nse Products, Inc.
Labeler Code:
62839
Product Label ID:
33fcd7e6-598b-46af-9259-93c40bf61610
Start Marketing Date: [9]
09-01-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 62839-1133?

The NDC code 62839-1133 is assigned by the FDA to the product Sunright Bodyblock Spf15 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 62839-1133-1 100 ml 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 Sunright Bodyblock Spf15?

Adults and children 6 months of age and over: Apply evenly 30 minutes before sun or water exposure. Reapply after swimming or excessive perspiring or anytime after towel drying. Children under 2 years of age: Use sunscreen products with a minimum SPF of 4. Children under 6 months of age: consult a doctor. Note: As with similar products, avoid immediate contact with natural fibers upon application.

Which are Sunright Bodyblock Spf15 UNII Codes?

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

Which are Sunright Bodyblock Spf15 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".