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  4. NDC Product Code: 90114-303 50 Pack Antibacterial Hand Wipes - Aloe

NDC 90114-303 50 Pack Antibacterial Hand Wipes - Aloe

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 90114-303?
  5. 50 Pack Antibacterial Hand Wipes - Aloe 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:
90114-303
Proprietary Name:
50 Pack Antibacterial Hand Wipes - Aloe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hero Brands, Inc.
Labeler Code:
90114
Product Label ID:
adc160e8-6e23-31bf-e053-2a95a90a1a74
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 90114-303-01

Package Description: 50 CLOTH in 1 BAG

Product Details

What is NDC 90114-303?

The NDC code 90114-303 is assigned by the FDA to the product 50 Pack Antibacterial Hand Wipes - Aloe which is product labeled by Hero Brands, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 90114-303-01 50 cloth in 1 bag . 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 50 Pack Antibacterial Hand Wipes - Aloe?

Wet hands thoroughly with product and allow to dry.Children under 6 years of age should be supervised when using product.

Which are 50 Pack Antibacterial Hand Wipes - Aloe UNII Codes?

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

Which are 50 Pack Antibacterial Hand Wipes - Aloe 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:

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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".