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  4. NDC Product Code: 75847-1713 Dr. Iaso Ac Booster

NDC 75847-1713 Dr. Iaso Ac Booster

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75847-1713?
  4. Dr. Iaso Ac Booster 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:
75847-1713
Proprietary Name:
Dr. Iaso Ac Booster
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Iaso Inc
Labeler Code:
75847
Product Label ID:
404685fb-9b4a-1fe1-e054-00144ff8d46c
Start Marketing Date: [9]
08-01-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 75847-1713-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 75847-1713?

The NDC code 75847-1713 is assigned by the FDA to the product Dr. Iaso Ac Booster which is product labeled by Iaso Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75847-1713-1 30 ml in 1 bottle, dropper . 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 Dr. Iaso Ac Booster?

Gently apply an appropriate amount to the skin.Follow with your serum and moisturizer.

Which are Dr. Iaso Ac Booster UNII Codes?

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

Which are Dr. Iaso Ac Booster 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".