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  4. NDC Product Code: 70908-180 Mefactory Super Light Cleansing

NDC 70908-180 Mefactory Super Light Cleansing

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70908-180?
  4. Mefactory Super Light Cleansing 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:
70908-180
Proprietary Name:
Mefactory Super Light Cleansing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mefactory Co., Ltd.
Labeler Code:
70908
Product Label ID:
0d26e5ee-295e-4eeb-890a-75bec9fee620
Start Marketing Date: [9]
12-01-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 70908-180?

The NDC code 70908-180 is assigned by the FDA to the product Mefactory Super Light Cleansing which is product labeled by Mefactory Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70908-180-01 200 ml in 1 bottle, pump . 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 Mefactory Super Light Cleansing?

Directions: 1. Apply oil cleanser into the palms of your dry hands 2. Apply the oil cleanser to your dry face by rubbing your hands on your entire face and remove makeup 3.Wash off the oil cleanser with warm water

Which are Mefactory Super Light Cleansing UNII Codes?

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

Which are Mefactory Super Light Cleansing 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".