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  4. NDC Product Code: 80546-001 Sanitized Pro Multi-purpose Antibacterial Wipes

NDC 80546-001 Sanitized Pro Multi-purpose Antibacterial Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80546-001?
  4. Sanitized Pro Multi-purpose Antibacterial Wipes Uses
  5. Active Ingredients UNII Codes
  6. 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:
80546-001
Proprietary Name:
Sanitized Pro Multi-purpose Antibacterial Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Poseidon Technology, Llc
Labeler Code:
80546
Product Label ID:
af09c081-a819-da13-e053-2a95a90a317b
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 80546-001?

The NDC code 80546-001 is assigned by the FDA to the product Sanitized Pro Multi-purpose Antibacterial Wipes which is product labeled by Poseidon Technology, Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 80546-001-16 800 g in 1 canister , 80546-001-50 2500 g in 1 canister , 80546-001-80 400 g 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 Sanitized Pro Multi-purpose Antibacterial Wipes?

Adults and children 2 years and over: Apply to area and allow to dry without wiping. Children should be supervised when using and those under 2 years of age ask doctor before use. Do not flush. Discard in a trash receptacle.

Which are Sanitized Pro Multi-purpose Antibacterial Wipes UNII Codes?

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

Which are Sanitized Pro Multi-purpose 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:

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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".