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  4. NDC Product Code: 73312-010 Fill Me Micro Needle

NDC 73312-010 Fill Me Micro Needle

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73312-010?
  4. Fill Me Micro Needle 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:
73312-010
Proprietary Name:
Fill Me Micro Needle
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jys Tech Co.,ltd
Labeler Code:
73312
Product Label ID:
31e7225c-8a5a-43cd-a4b8-ac8d053c4466
Start Marketing Date: [9]
08-01-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 73312-010?

The NDC code 73312-010 is assigned by the FDA to the product Fill Me Micro Needle which is product labeled by Jys Tech Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73312-010-02 8 container in 1 carton / .55 g in 1 container (73312-010-01). 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 Fill Me Micro Needle?

Directions:1) Before sleep, cleanse your face and remove water.2) Open the pouch and plastic case carefully.3) Be careful not to touch the center area with fingers and remove white protective film.4) Attach patches on the area you want and press vertically with fingers for about 1 minute.5) Peel softly in next morning. (or after 2 hours minimum)

Which are Fill Me Micro Needle UNII Codes?

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

Which are Fill Me Micro Needle 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".