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  4. NDC Product Code: 71496-0002 Energy Boosting Toner

NDC 71496-0002 Energy Boosting Toner

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71496-0002?
  4. Energy Boosting Toner 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:
71496-0002
Proprietary Name:
Energy Boosting Toner
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ari&j Inc
Labeler Code:
71496
Product Label ID:
538a6075-6d27-095d-e054-00144ff8d46c
Start Marketing Date: [9]
07-05-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 71496-0002?

The NDC code 71496-0002 is assigned by the FDA to the product Energy Boosting Toner which is product labeled by Ari&j Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71496-0002-1 160 ml in 1 bottle . 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 Energy Boosting Toner?

After cleansing your face, apply an appropriate amount with the clean palms until the product absorbs completely.When using a cotton pad, pour enough amount to wet the cotton pad and clean off any left residues on your skin after cleansing from inside to outside.

Which are Energy Boosting Toner UNII Codes?

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

Which are Energy Boosting Toner 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".