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  4. NDC Product Code: 74617-045 Goodhands Alcohol Wipes

NDC 74617-045 Goodhands Alcohol Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 74617-045?
  4. Goodhands 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:
74617-045
Proprietary Name:
Goodhands Alcohol Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Symn Industries, Llc
Labeler Code:
74617
Product Label ID:
b2476cda-7bc2-08c2-e053-2995a90a0cb4
Start Marketing Date: [9]
10-22-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 74617-045?

The NDC code 74617-045 is assigned by the FDA to the product Goodhands Alcohol Wipes which is product labeled by Symn Industries, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 74617-045-01 100 canister in 1 canister / 600 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 Goodhands Alcohol Wipes?

Unsnap entire canister cap and thread middle roll of wipe through pre-cut slot.Pull wipe out of cap slot at an angle to dispense.Wet hands and wrists thoroughly with wipes for 15 seconds and allow to air dry.Can use on general cleaning areas and wipe down to clean thoroughly.Dispose of used wipe in trash after use. Do not flush.Always reseal after use to keep moisture.Children under 6 years of age should be supervised when using this product.

Which are Goodhands Alcohol Wipes UNII Codes?

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

Which are Goodhands 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 Goodhands 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".