1. Home
  2. Labeler Index
  3. Kangna (zhejiang) Medical Supplies Co., Ltd.
  4. NDC Product Code: 75109-507 Alcosm Antibacterial Wipes

NDC 75109-507 Alcosm Antibacterial Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 75109-507?
  5. Alcosm Antibacterial Wipes Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
75109-507
Proprietary Name:
Alcosm Antibacterial Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kangna (zhejiang) Medical Supplies Co., Ltd.
Labeler Code:
75109
Product Label ID:
a9bc0a27-d4e5-7a9d-e053-2995a90a21b0
Start Marketing Date: [9]
07-05-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
LEMON (C73396)

Code Structure Chart

Product Details

What is NDC 75109-507?

The NDC code 75109-507 is assigned by the FDA to the product Alcosm Antibacterial Wipes which is product labeled by Kangna (zhejiang) Medical Supplies Co., Ltd.. The product's dosage form is . The product is distributed in 9 packages with assigned NDC codes 75109-507-01 600 package in 1 carton / 1 not applicable in 1 package / 5.5 g in 1 not applicable, 75109-507-02 100 package in 1 carton / 10 not applicable in 1 package / 58 g in 1 not applicable, 75109-507-03 24 package in 1 carton / 50 not applicable in 1 package / 270 g in 1 not applicable, 75109-507-04 16 package in 1 carton / 80 not applicable in 1 package / 430 g in 1 not applicable, 75109-507-05 16 package in 1 carton / 100 not applicable in 1 package / 530 g in 1 not applicable, 75109-507-06 12 canister in 1 carton / 75 not applicable in 1 canister / 420 g in 1 not applicable, 75109-507-07 12 canister in 1 carton / 150 not applicable in 1 canister / 420 g in 1 not applicable, 75109-507-08 12 canister in 1 carton / 240 not applicable in 1 canister / 760 g in 1 not applicable, 75109-507-09 2 canister in 1 carton / 350 not applicable in 1 canister / 2768 g in 1 not applicable. 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 Alcosm Antibacterial Wipes?

Remove lid. Pull wipe from center of roll and thread through opening in lid. Do not push finger through opening. Replace lid, pull wipe up and then out at 45° angle. Next wipe dispenses automatically. Close lid to retain moisture.

Which are Alcosm Antibacterial Wipes UNII Codes?

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

Which are Alcosm Antibacterial 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 Alcosm Antibacterial 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:

* 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".