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  4. NDC Product Code: 75109-513 Alcosm Alcohol Wipes

NDC 75109-513 Alcosm Alcohol Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75109-513?
  4. Alcosm 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:
75109-513
Proprietary Name:
Alcosm Alcohol 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:
aa5dc806-4ced-1dde-e053-2995a90a2961
Start Marketing Date: [9]
07-05-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 75109-513-01

Package Description: 12 BOX in 1 CARTON / 50 PACKAGE in 1 BOX / 1 NOT APPLICABLE in 1 PACKAGE / 2.8 mL in 1 NOT APPLICABLE

NDC Code 75109-513-02

Package Description: 100 PACKAGE in 1 CARTON / 10 NOT APPLICABLE in 1 PACKAGE / 37.8 mL in 1 NOT APPLICABLE

NDC Code 75109-513-03

Package Description: 24 PACKAGE in 1 CASE / 50 NOT APPLICABLE in 1 PACKAGE / 189 mL in 1 NOT APPLICABLE

NDC Code 75109-513-04

Package Description: 16 PACKAGE in 1 CARTON / 80 NOT APPLICABLE in 1 PACKAGE / 302.4 mL in 1 NOT APPLICABLE

NDC Code 75109-513-05

Package Description: 16 PACKAGE in 1 CARTON / 100 NOT APPLICABLE in 1 PACKAGE / 378 mL in 1 NOT APPLICABLE

NDC Code 75109-513-06

Package Description: 12 BOX in 1 CARTON / 100 PACKAGE in 1 BOX / 1 NOT APPLICABLE in 1 PACKAGE / 2 mL in 1 NOT APPLICABLE

NDC Code 75109-513-07

Package Description: 24 BOX in 1 CARTON / 50 PACKAGE in 1 BOX / 1 NOT APPLICABLE in 1 PACKAGE / 2 mL in 1 NOT APPLICABLE

NDC Code 75109-513-08

Package Description: 200 PACKAGE in 1 BOX / 1 NOT APPLICABLE in 1 PACKAGE / 2 mL in 1 NOT APPLICABLE

NDC Code 75109-513-09

Package Description: 12 CANISTER in 1 CARTON / 75 NOT APPLICABLE in 1 CANISTER / 258.825 mL in 1 NOT APPLICABLE

NDC Code 75109-513-10

Package Description: 12 CANISTER in 1 CARTON / 150 NOT APPLICABLE in 1 CANISTER / 235.2 mL in 1 NOT APPLICABLE

NDC Code 75109-513-11

Package Description: 12 CANISTER in 1 CARTON / 240 NOT APPLICABLE in 1 CANISTER / 471.59884 mL in 1 NOT APPLICABLE

NDC Code 75109-513-12

Package Description: 2 CANISTER in 1 CARTON / 350 NOT APPLICABLE in 1 CANISTER / 1796.258 mL in 1 NOT APPLICABLE

NDC Code 75109-513-13

Package Description: 4 PACKAGE in 1 CARTON / 800 NOT APPLICABLE in 1 PACKAGE / 1515.136 mL in 1 NOT APPLICABLE

Product Details

What is NDC 75109-513?

The NDC code 75109-513 is assigned by the FDA to the product Alcosm Alcohol Wipes which is product labeled by Kangna (zhejiang) Medical Supplies Co., Ltd.. The product's dosage form is . The product is distributed in 13 packages with assigned NDC codes 75109-513-01 12 box in 1 carton / 50 package in 1 box / 1 not applicable in 1 package / 2.8 ml in 1 not applicable, 75109-513-02 100 package in 1 carton / 10 not applicable in 1 package / 37.8 ml in 1 not applicable, 75109-513-03 24 package in 1 case / 50 not applicable in 1 package / 189 ml in 1 not applicable, 75109-513-04 16 package in 1 carton / 80 not applicable in 1 package / 302.4 ml in 1 not applicable, 75109-513-05 16 package in 1 carton / 100 not applicable in 1 package / 378 ml in 1 not applicable, 75109-513-06 12 box in 1 carton / 100 package in 1 box / 1 not applicable in 1 package / 2 ml in 1 not applicable, 75109-513-07 24 box in 1 carton / 50 package in 1 box / 1 not applicable in 1 package / 2 ml in 1 not applicable, 75109-513-08 200 package in 1 box / 1 not applicable in 1 package / 2 ml in 1 not applicable, 75109-513-09 12 canister in 1 carton / 75 not applicable in 1 canister / 258.825 ml in 1 not applicable, 75109-513-10 12 canister in 1 carton / 150 not applicable in 1 canister / 235.2 ml in 1 not applicable, 75109-513-11 12 canister in 1 carton / 240 not applicable in 1 canister / 471.59884 ml in 1 not applicable, 75109-513-12 2 canister in 1 carton / 350 not applicable in 1 canister / 1796.258 ml in 1 not applicable, 75109-513-13 4 package in 1 carton / 800 not applicable in 1 package / 1515.136 ml 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 Alcohol 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 Alcohol Wipes UNII Codes?

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

Which are Alcosm 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 Alcosm 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".