NDC 72910-0003 Funees

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72910-0003
Proprietary Name:
Funees
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ds Tech Co., Ltd
Labeler Code:
72910
Start Marketing Date: [9]
07-21-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72910-0003-1

Package Description: 68 g in 1 PATCH

Product Details

What is NDC 72910-0003?

The NDC code 72910-0003 is assigned by the FDA to the product Funees which is product labeled by Ds Tech Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72910-0003-1 68 g in 1 patch . 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 Funees?

Spread water soluble cosmetics all over your face before usingopen one sterilized micro chip roller for usepress the left pushbutton of the dedicated roller handle to insert a micro chip rollergently rolls massages along the fact surface from inside to outsideuse only until you feel no stimulation from the micro chipafter using, apply cosmetics evenly across faceafter using, press the roller handle depressor to discard the micro chip roller (the micro chip roller is disposable)dedicated roller handle keeps it clean with a continous use product(this product is recommended to use one every 2 to 3 days)

Which are Funees UNII Codes?

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

Which are Funees 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".