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  4. NDC Product Code: 58418-274 Eco Spf30 Sun Stick

NDC 58418-274 Eco Spf30 Sun Stick

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 58418-274?
  5. Eco Spf30 Sun Stick 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:
58418-274
Proprietary Name:
Eco Spf30 Sun Stick
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tropical Enterprises International, Inc
Labeler Code:
58418
Product Label ID:
747354f2-ee2c-1279-e053-2a91aa0aa707
Start Marketing Date: [9]
08-01-2014
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 58418-274?

The NDC code 58418-274 is assigned by the FDA to the product Eco Spf30 Sun Stick which is product labeled by Tropical Enterprises International, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58418-274-05 15 ml in 1 canister . 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 Eco Spf30 Sun Stick?

This product is used as UsesHelps prevent sunburnIf used as directed with other sun protection measures (see Cirections), decreases the risk of skin cancer and early skin aging caused by the sun.

Which are Eco Spf30 Sun Stick UNII Codes?

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

Which are Eco Spf30 Sun Stick 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".