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  4. NDC Product Code: 51531-9480 Lip Protector Sunscreen Spf15

NDC 51531-9480 Lip Protector Sunscreen Spf15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51531-9480?
  4. Lip Protector Sunscreen 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:
51531-9480
Proprietary Name:
Lip Protector Sunscreen Spf15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mary Kay Inc.
Labeler Code:
51531
Product Label ID:
376f984e-0ecb-489b-9b76-c77b4416f04a
Start Marketing Date: [9]
03-01-2007
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 51531-9480?

The NDC code 51531-9480 is assigned by the FDA to the product Lip Protector Sunscreen Spf15 which is product labeled by Mary Kay Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51531-9480-0 4.5 g in 1 container . 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 Lip Protector Sunscreen Spf15?

DIRECTION: Apply liberally at least 15 minutes before sun exposure, alone or under lipstick. Reapply every one to three hours as needed and after swimming, eating or drinking .3

Which are Lip Protector Sunscreen Spf15 UNII Codes?

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

Which are Lip Protector Sunscreen 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".