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  4. NDC Product Code: 74658-013 Alcohol Wipes

NDC 74658-013 Alcohol Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 74658-013?
  4. Alcohol Wipes Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
74658-013
Proprietary Name:
Alcohol Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Guangzhou Xuelei Cosmetic Co.,ltd.
Labeler Code:
74658
Product Label ID:
b69f2109-0e1d-9924-e053-2995a90a9b50
Start Marketing Date: [9]
10-10-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 74658-013-01

Package Description: 1 PATCH in 1 BAG / 4.3 mL in 1 PATCH

NDC Code 74658-013-02

Package Description: 75 PATCH in 1 BOTTLE / 4.3 mL in 1 PATCH

NDC Code 74658-013-03

Package Description: 80 PATCH in 1 BOTTLE / 4.3 mL in 1 PATCH

NDC Code 74658-013-04

Package Description: 100 PATCH in 1 BOTTLE / 4.3 mL in 1 PATCH

NDC Code 74658-013-05

Package Description: 120 PATCH in 1 BOTTLE / 4.3 mL in 1 PATCH

NDC Code 74658-013-06

Package Description: 130 PATCH in 1 BOTTLE / 4.3 mL in 1 PATCH

NDC Code 74658-013-07

Package Description: 150 PATCH in 1 BOTTLE / 4.3 mL in 1 PATCH

NDC Code 74658-013-08

Package Description: 180 PATCH in 1 BOTTLE / 4.3 mL in 1 PATCH

NDC Code 74658-013-09

Package Description: 200 PATCH in 1 BOTTLE / 4.3 mL in 1 PATCH

Product Details

What is NDC 74658-013?

The NDC code 74658-013 is assigned by the FDA to the product Alcohol Wipes which is product labeled by Guangzhou Xuelei Cosmetic Co.,ltd.. The product's dosage form is . The product is distributed in 9 packages with assigned NDC codes 74658-013-01 1 patch in 1 bag / 4.3 ml in 1 patch, 74658-013-02 75 patch in 1 bottle / 4.3 ml in 1 patch, 74658-013-03 80 patch in 1 bottle / 4.3 ml in 1 patch, 74658-013-04 100 patch in 1 bottle / 4.3 ml in 1 patch, 74658-013-05 120 patch in 1 bottle / 4.3 ml in 1 patch, 74658-013-06 130 patch in 1 bottle / 4.3 ml in 1 patch, 74658-013-07 150 patch in 1 bottle / 4.3 ml in 1 patch, 74658-013-08 180 patch in 1 bottle / 4.3 ml in 1 patch, 74658-013-09 200 patch in 1 bottle / 4.3 ml in 1 patch. 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 Alcohol Wipes?

1、OPEN THE BARREL CAP;2、RIVE THE SEAL;3、PULL OUT THE WET TISSUE TOWEL THROUGH SMALL OPENING;4、COVER THE LIP;5、RUB THOROUGHLY OVER ALL SURFACES OF BOTH HANDS WITH THE WET WIPES;6、ALLOW TO DRY WITHOUT WIPING;7、DISPOSE OF WIPES IN TRASH AFTER USE. DOT NOT FLUSH.

Which are Alcohol Wipes UNII Codes?

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

Which are Alcohol 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:

What is the NDC to RxNorm Crosswalk for Alcohol Wipes?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".