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  4. NDC Product Code: 59427-728 Rain And Shine Liptint With Spf 10 Sunscreen

NDC 59427-728 Rain And Shine Liptint With Spf 10 Sunscreen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59427-728?
  4. 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:
59427-728
Proprietary Name:
Rain And Shine Liptint With Spf 10 Sunscreen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Origins Natural Resources Inc
Labeler Code:
59427
Product Label ID:
6e510db9-4253-4813-9a4d-2399d722d5bb
Start Marketing Date: [9]
09-01-2001
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 59427-728?

The NDC code 59427-728 is assigned by the FDA to the product Rain And Shine Liptint With Spf 10 Sunscreen which is product labeled by Origins Natural Resources Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59427-728-01 1 cartridge in 1 carton / 2.5 g in 1 cartridge (59427-728-02). 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.

Which are Rain And Shine Liptint With Spf 10 Sunscreen UNII Codes?

The UNII codes for the active 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".