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  4. NDC Product Code: 40905-002 Wet Tissue With Alcohol 75%

NDC 40905-002 Wet Tissue With Alcohol 75%

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 40905-002?
  5. Wet Tissue With Alcohol 75% Uses
  6. Active Ingredients UNII Codes
  7. 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:
40905-002
Proprietary Name:
Wet Tissue With Alcohol 75%
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jiangxi Hualida Industrial Co., Ltd.
Labeler Code:
40905
Product Label ID:
a582fc64-5730-d269-e053-2a95a90af7dd
Start Marketing Date: [9]
04-14-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Size(s):
95 MM

Code Structure Chart

Product Details

What is NDC 40905-002?

The NDC code 40905-002 is assigned by the FDA to the product Wet Tissue With Alcohol 75% which is product labeled by Jiangxi Hualida Industrial Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 40905-002-01 50 cloth in 1 package . 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 Wet Tissue With Alcohol 75%?

Wipe gently with wet tissues on hands。

Which are Wet Tissue With Alcohol 75% UNII Codes?

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

Which are Wet Tissue With Alcohol 75% 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".