1. Home
  2. Labeler Index
  3. Island Company Lifestyle Products, Llc
  4. NDC Product Code: 10755-015 Traveler Spf15

NDC 10755-015 Traveler Spf15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 10755-015?
  4. Traveler 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:
10755-015
Proprietary Name:
Traveler Spf15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Island Company Lifestyle Products, Llc
Labeler Code:
10755
Product Label ID:
dda17405-2e3c-46ac-9614-5278933d540c
Start Marketing Date: [9]
08-01-2009
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 10755-015-02

Package Description: 59 g in 1 BOTTLE

NDC Code 10755-015-08

Package Description: 236 g in 1 BOTTLE

Product Details

What is NDC 10755-015?

The NDC code 10755-015 is assigned by the FDA to the product Traveler Spf15 which is product labeled by Island Company Lifestyle Products, Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 10755-015-02 59 g in 1 bottle , 10755-015-08 236 g in 1 bottle . 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 Traveler Spf15?

Apply liberally 20 minutes before sun exposure and as neededFor children under 6 months of age: Ask a doctor

Which are Traveler Spf15 UNII Codes?

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

Which are Traveler 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:

* Please review the disclaimer below.

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".