NDC 71164-020 Mu Lab Turn Around 2w Refresh Ex

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:
71164-020
Proprietary Name:
Mu Lab Turn Around 2w Refresh Ex
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mu-biz.co,.ltd
Labeler Code:
71164
Start Marketing Date: [9]
12-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71164-020-02

Package Description: 1 TUBE in 1 CARTON / 20 mL in 1 TUBE (71164-020-01)

Product Details

What is NDC 71164-020?

The NDC code 71164-020 is assigned by the FDA to the product Mu Lab Turn Around 2w 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 71164-020-02 1 tube in 1 carton / 20 ml in 1 tube (71164-020-01). 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 Turn Around 2w Refresh Ex?

Directions: - Clean the skin thoroughly before using - Day and night, apply amount of one pumping onto forehead and nose, and massage in the order of forehead, nose->cheeks->eyes. The active ingredients are highly concentrated and need to be controlled in this way. The first area to come in contact with this product will be the most effected. So, for instance, apply the designated amount first around the eyes may irritate. Massage lightly. If no irritation is visible, increase amount through a 3-to-4-day interval.

Which are Mu Lab Turn Around 2w Refresh Ex UNII Codes?

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

Which are Mu Lab Turn Around 2w 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".