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NDC 66134-060 Safe Sea Spf 60

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 66134-060?
  4. Safe Sea Spf 60 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:
66134-060
Proprietary Name:
Safe Sea Spf 60
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sasa Cosmetics
Labeler Code:
66134
Product Label ID:
cb6f18fe-35ef-4145-908f-0e9b6cd27754
Start Marketing Date: [9]
01-07-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 66134-060-60

Package Description: 118 g in 1 TUBE

Product Details

What is NDC 66134-060?

The NDC code 66134-060 is assigned by the FDA to the product Safe Sea Spf 60 which is product labeled by Sasa Cosmetics. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66134-060-60 118 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 Safe Sea Spf 60?

Uses: Helps prevent sunburn -- If used as directed with other sunprotection measures ( see directions), decreases the risk of skin cancerand early skin aging caused by the sun

Which are Safe Sea Spf 60 UNII Codes?

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

Which are Safe Sea Spf 60 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".