NDC 72144-030 Dr Jmeelab Double Complex Smile Zone

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:
72144-030
Proprietary Name:
Dr Jmeelab Double Complex Smile Zone
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jmpbio Co., Ltd.
Labeler Code:
72144
Start Marketing Date: [9]
02-01-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72144-030-02

Package Description: 10 POUCH in 1 CARTON / 5 mL in 1 POUCH (72144-030-01)

Product Details

What is NDC 72144-030?

The NDC code 72144-030 is assigned by the FDA to the product Dr Jmeelab Double Complex Smile Zone which is product labeled by Jmpbio Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72144-030-02 10 pouch in 1 carton / 5 ml in 1 pouch (72144-030-01). 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 Dr Jmeelab Double Complex Smile Zone?

Directions:1. Apply toner after cleansing. Detach film from STEP 1 Smile-zone Patch and attach it to area or concern including eye and lip areas. 2. After confirming the patch has been attached well, detach film from STEP 2 Black Mast and attach it to face. 3. After taking a rest for 10~20 minutes, detach mask sheet and patch. Tap lightly to help remaining essence be absorbed fully.

Which are Dr Jmeelab Double Complex Smile Zone UNII Codes?

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

Which are Dr Jmeelab Double Complex Smile Zone 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".