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NDC 71164-010 Mu Lab Yeco Solu Tion Bp Refresh Ex

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71164-010?
  4. Mu Lab Yeco Solu Tion Bp Refresh Ex 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:
71164-010
Proprietary Name:
Mu Lab Yeco Solu Tion Bp Refresh Ex
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mu-biz.co,.ltd
Labeler Code:
71164
Product Label ID:
f76a296c-6139-4c05-a3f0-165d02db87a9
Start Marketing Date: [9]
12-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 71164-010?

The NDC code 71164-010 is assigned by the FDA to the product Mu Lab Yeco Solu Tion Bp Refresh Ex which is product labeled by Mu-biz.co,.ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71164-010-02 1 bottle, plastic in 1 carton / 25 ml in 1 bottle, plastic (71164-010-01). 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 Mu Lab Yeco Solu Tion Bp Refresh Ex?

Directions: -Use in the morning and at night. -For the first few times, test product with two droplets on forehead and nose. -If the product agrees with your skin, apply 2 to 3 more droplets on areas with visible pores. -If there is no irritation, increase amount by 1 to 2 droplets per every 3 to 4 days. -Those with oily skin but do not use makeup can also use this during the day. - Clean the skin thoroughly before using - Apply in daily skin care routine

Which are Mu Lab Yeco Solu Tion Bp Refresh Ex UNII Codes?

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

Which are Mu Lab Yeco Solu Tion Bp Refresh Ex 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".