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  4. NDC Product Code: 71974-040 Skinmd Laboratories Revitox Blue

NDC 71974-040 Skinmd Laboratories Revitox Blue

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71974-040?
  4. Skinmd Laboratories Revitox Blue 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:
71974-040
Proprietary Name:
Skinmd Laboratories Revitox Blue
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Reviresco Co., Ltd.
Labeler Code:
71974
Product Label ID:
ad87d4f8-e195-40a8-b17b-36e8e5817719
Start Marketing Date: [9]
12-01-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71974-040-02

Package Description: 10 VIAL in 1 CARTON / 10 mL in 1 VIAL (71974-040-01)

Product Details

What is NDC 71974-040?

The NDC code 71974-040 is assigned by the FDA to the product Skinmd Laboratories Revitox Blue which is product labeled by Reviresco Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71974-040-02 10 vial in 1 carton / 10 ml in 1 vial (71974-040-01). 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 Skinmd Laboratories Revitox Blue?

Directions: 1. Clean your face carefully and remove the water remains. 2. Open the lid of the vial. 3. Put the transparent lid which can be found in the box on the solution bottle. 4. Take 2cc Revitoxblue solution on the back of your hand. 5. Smear Revitoxblue solution on the face where you want and pat the face to help absorb. 6. After using, please cover the transparent lid and store it in refrigerator. 7. Using it every morning and night.

Which are Skinmd Laboratories Revitox Blue UNII Codes?

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

Which are Skinmd Laboratories Revitox Blue 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".