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NDC 82363-020 Medioro Signature Essence Mist

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82363-020?
  4. Medioro Signature Essence Mist 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:
82363-020
Proprietary Name:
Medioro Signature Essence Mist
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Medifun Inc.
Labeler Code:
82363
Product Label ID:
c0b843a8-9eb2-4eac-b638-4a1e874ef768
Start Marketing Date: [9]
06-01-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 82363-020?

The NDC code 82363-020 is assigned by the FDA to the product Medioro Signature Essence Mist which is product labeled by Medifun Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82363-020-02 1 bottle, spray in 1 carton / 160 ml in 1 bottle, spray (82363-020-01). 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 Medioro Signature Essence Mist?

■ Spray lightly about 10cm away from the area of use.■ You can use if from time to time if necessary.■ It helps when your skin is dry.

Which are Medioro Signature Essence Mist UNII Codes?

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

Which are Medioro Signature Essence Mist 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".