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  4. NDC Product Code: 67038-110 The Youth As We Know It

NDC 67038-110 The Youth As We Know It

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 67038-110?
  4. The Youth As We Know It 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:
67038-110
Proprietary Name:
The Youth As We Know It
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bliss World Llc
Labeler Code:
67038
Product Label ID:
e026e1c6-19d0-4870-b277-74124a1d4a44
Start Marketing Date: [9]
02-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 67038-110-50

Package Description: 15 mL in 1 TUBE

NDC Code 67038-110-51

Package Description: 50 mL in 1 TUBE

Product Details

What is NDC 67038-110?

The NDC code 67038-110 is assigned by the FDA to the product The Youth As We Know It which is product labeled by Bliss World Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 67038-110-50 15 ml in 1 tube , 67038-110-51 50 ml 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 The Youth As We Know It?

DirectionsApply generously and evenly 20 minutes before sun exposureChildren under 6 months of age ask a doctorReapply as needed or after towel drying, swimming, or prespiring

Which are The Youth As We Know It UNII Codes?

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

Which are The Youth As We Know It 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".