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  4. NDC Product Code: 55118-600 Sunscreen Mango And Coconut

NDC 55118-600 Sunscreen Mango And Coconut

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 55118-600?
  4. Sunscreen Mango And Coconut Uses
  5. Active 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:
55118-600
Proprietary Name:
Sunscreen Mango And Coconut
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kimberly-clark Corporation
Labeler Code:
55118
Product Label ID:
aff60363-62f7-476c-accb-032e28e82793
Start Marketing Date: [9]
03-15-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 55118-600?

The NDC code 55118-600 is assigned by the FDA to the product Sunscreen Mango And Coconut which is product labeled by Kimberly-clark Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55118-600-11 45 g in 1 bottle, plastic . 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 Sunscreen Mango And Coconut?

Apply generously 15 minutes before sun exposure and as needed.Reapply as needed or after towel drying, swimming or sweating.Ask a doctor before use on children under six months of age.

Which are Sunscreen Mango And Coconut UNII Codes?

The UNII codes for the active 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".