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  4. NDC Product Code: 70018-010 Hyaluronic Acid Micro

NDC 70018-010 Hyaluronic Acid Micro

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70018-010?
  4. Hyaluronic Acid Micro 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:
70018-010
Proprietary Name:
Hyaluronic Acid Micro
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Junmok International,inc
Labeler Code:
70018
Product Label ID:
9aa06328-b8c2-47b7-9281-15e4da8f2745
Start Marketing Date: [9]
07-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 70018-010?

The NDC code 70018-010 is assigned by the FDA to the product Hyaluronic Acid Micro which is product labeled by Junmok International,inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70018-010-01 4 patch 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 Hyaluronic Acid Micro?

Indications & usage:1. Take a patch out of the pouch with dry hand after face washing. 2. Try not to touch the middle side (needle) and take off the protective film carefully. 3. Place and attach the middle side of the patch on a desired area vertically. 4. Press the middle part of the patch attached with fingers several times. 5. Go to bed with patch attached and take it off the next morning.

Which are Hyaluronic Acid Micro UNII Codes?

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

Which are Hyaluronic Acid Micro 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".