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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.

Get all the details for National Drug Code (NDC) 71164-010 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

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
FDA Application Number: [6]
part333D
Marketing Category: [8]
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date: [9]
12-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

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.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".