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  4. NDC Product Code: 54473-168 Sun Shades Lip Balm Pomegranate Spf 15

NDC 54473-168 Sun Shades Lip Balm Pomegranate Spf 15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 54473-168?
  5. Sun Shades Lip Balm Pomegranate Spf 15 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:
54473-168
Proprietary Name:
Sun Shades Lip Balm Pomegranate Spf 15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Melaleuca, Inc.
Labeler Code:
54473
Product Label ID:
5bc60cf9-675e-4cfe-b96e-40a349705af8
Start Marketing Date: [9]
10-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
POMEGRANATE (C73411 - POMEGRANATE)

Code Structure Chart

Product Details

What is NDC 54473-168?

The NDC code 54473-168 is assigned by the FDA to the product Sun Shades Lip Balm Pomegranate Spf 15 which is product labeled by Melaleuca, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54473-168-01 4.2 g in 1 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 Sun Shades Lip Balm Pomegranate Spf 15?

This product is used as Uses:  Helps protect against sunburn.

Which are Sun Shades Lip Balm Pomegranate Spf 15 UNII Codes?

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

Which are Sun Shades Lip Balm Pomegranate Spf 15 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".