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  4. NDC Product Code: 62217-152 Presidents Choice

NDC 62217-152 Presidents Choice

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62217-152?
  4. Presidents Choice 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:
62217-152
Proprietary Name:
Presidents Choice
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Fruit Of The Earth, Inc.
Labeler Code:
62217
Product Label ID:
f7c4869b-d68d-423c-94cf-221ffa5e7f4d
Start Marketing Date: [9]
03-30-2005
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 62217-152-23

Package Description: 220 g in 1 TUBE

Product Details

What is NDC 62217-152?

The NDC code 62217-152 is assigned by the FDA to the product Presidents Choice which is product labeled by Fruit Of The Earth, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62217-152-23 220 g in 1 tube . 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 Presidents Choice?

Enter section text hereApply liberally 15 to 30 minutes before sun exposure.  Reapply after swimming, excessive perspiration or washing.The sun may cause sunburn, premature aging of the skin and skin cancer.  Avoiding the sun, wearing protective clothing and regular use of sunscreens over the years may reduce the chance of these harmful effects.

Which are Presidents Choice 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".