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  4. NDC Product Code: 71496-0001 Moisture Bound

NDC 71496-0001 Moisture Bound

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71496-0001?
  4. Moisture Bound 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:
71496-0001
Proprietary Name:
Moisture Bound
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ari&j Inc
Labeler Code:
71496
Product Label ID:
5389c38c-3090-602e-e054-00144ff8d46c
Start Marketing Date: [9]
07-05-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71496-0001-1

Package Description: 50 mL in 1 JAR

Product Details

What is NDC 71496-0001?

The NDC code 71496-0001 is assigned by the FDA to the product Moisture Bound 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 71496-0001-1 50 ml in 1 jar . 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 Moisture Bound?

After Cleansing your face, apply after applying serum.Can be used as a mask when applied generously.

Which are Moisture Bound UNII Codes?

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

Which are Moisture Bound 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".