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  4. NDC Product Code: 75916-0660 Surfers Skin Sunscreen Lip Balm

NDC 75916-0660 Surfers Skin Sunscreen Lip Balm

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75916-0660?
  4. Surfers Skin Sunscreen Lip Balm 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:
75916-0660
Proprietary Name:
Surfers Skin Sunscreen Lip Balm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Skin Alive, Ltd.
Labeler Code:
75916
Product Label ID:
d49062c4-90b1-4db5-b616-1971fa628346
Start Marketing Date: [9]
01-17-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 75916-0660?

The NDC code 75916-0660 is assigned by the FDA to the product Surfers Skin Sunscreen Lip Balm which is product labeled by Skin Alive, Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75916-0660-8 1 tube, with applicator in 1 box / 8.5 g in 1 tube, with applicator. 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 Surfers Skin Sunscreen Lip Balm?

UsesHelps prevent sunburnHigher SPF gives more sunburn protectionProvides high protection against sunburnRegains SPF after 80 minutes of sweating.

Which are Surfers Skin Sunscreen Lip Balm UNII Codes?

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

Which are Surfers Skin Sunscreen Lip Balm 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".