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  4. NDC Product Code: 81940-001 Dark Spot Corrector

NDC 81940-001 Dark Spot Corrector

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81940-001?
  4. Dark Spot Corrector 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:
81940-001
Proprietary Name:
Dark Spot Corrector
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shenzhen Weikemo Intelligent Technology Co.,ltd
Labeler Code:
81940
Product Label ID:
c322f2d0-794d-5832-e053-2a95a90ae71a
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81940-001-01

Package Description: 50 g in 1 BOX

Product Details

What is NDC 81940-001?

The NDC code 81940-001 is assigned by the FDA to the product Dark Spot Corrector which is product labeled by Shenzhen Weikemo Intelligent Technology Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81940-001-01 50 g in 1 box . 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 Dark Spot Corrector?

1.Best to use in the morning and evening. 2.Recommended to use with an Sunscreen and moisture product. 3.Avoid contact with eyes.In case of accidental splash into eyes, please wash with clean water.Keep out of reach of infants and young children. 4.Stop use andask a doctor if irritation or rash occurs.These maybe signs of a serious condition.

Which are Dark Spot Corrector UNII Codes?

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

Which are Dark Spot Corrector 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:

* Please review the disclaimer below.

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".