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  4. NDC Product Code: 60781-1010 Thinksport Thinksun Sunscreen Spf 30

NDC 60781-1010 Thinksport Thinksun Sunscreen Spf 30

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 60781-1010?
  5. Thinksport Thinksun Sunscreen Spf 30 Uses
  6. Active Ingredients UNII Codes
  7. 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:
60781-1010
Proprietary Name:
Thinksport Thinksun Sunscreen Spf 30
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Thinkoperations,llc
Labeler Code:
60781
Product Label ID:
930bc7e2-5c12-45b8-98ef-287a302bf308
Start Marketing Date: [9]
01-01-2017
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 60781-1010?

The NDC code 60781-1010 is assigned by the FDA to the product Thinksport Thinksun Sunscreen Spf 30 which is product labeled by Thinkoperations,llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60781-1010-1 59 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 Thinksport Thinksun Sunscreen Spf 30?

Apply liberally 15 minutes before sun exposurereapplyafter 80 minutes of swimming or sweatingimmediately after towel dryingat least every two hours

Which are Thinksport Thinksun Sunscreen Spf 30 UNII Codes?

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

Which are Thinksport Thinksun Sunscreen Spf 30 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".