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  4. NDC Product Code: 81764-120 San Skinlab Cloth Wet Wipes

NDC 81764-120 San Skinlab Cloth Wet Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81764-120?
  4. San Skinlab Cloth Wet Wipes 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:
81764-120
Proprietary Name:
San Skinlab Cloth Wet Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bactec Co Ltd.
Labeler Code:
81764
Product Label ID:
bfd6a6aa-4250-ed7c-e053-2995a90a71af
Start Marketing Date: [9]
04-12-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81764-120-01

Package Description: 798 mL in 1 CANISTER

Product Details

What is NDC 81764-120?

The NDC code 81764-120 is assigned by the FDA to the product San Skinlab Cloth Wet Wipes which is product labeled by Bactec Co Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81764-120-01 798 ml in 1 canister . 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 San Skinlab Cloth Wet Wipes?

Wet hands thoroughly with product and allow to dry without wipingNot recommended for infants

Which are San Skinlab Cloth Wet Wipes UNII Codes?

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

Which are San Skinlab Cloth Wet Wipes 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".