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  4. NDC Product Code: 43071-120 Mirae Magic Balm

NDC 43071-120 Mirae Magic Balm

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43071-120?
  4. Mirae Magic Balm 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:
43071-120
Proprietary Name:
Mirae Magic Balm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Human And Nature
Labeler Code:
43071
Product Label ID:
64de95cb-9c33-40bc-ad2c-ad86202d96ca
Start Marketing Date: [9]
02-01-2016
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 43071-120?

The NDC code 43071-120 is assigned by the FDA to the product Mirae Magic Balm which is product labeled by Human And Nature. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43071-120-01 50 g in 1 carton . 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 Mirae Magic Balm?

Indications & usage: Skin care for extremely dry skin from all ages. Provides long-lasting moisture, increases resistance of the skin and can reduce itching. Spread evenly on skin after cleansing mornings and evenings and as needed. Depnding on the individual differences in the initial phase of use spots, dead skin cell, itching, burning etc –can be seen and happen. But these reactions may disappear and all fade away by way of your continuous use. So you don’t need to worry about it.

Which are Mirae Magic Balm UNII Codes?

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

Which are Mirae Magic Balm 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".