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  4. NDC Product Code: 63002-003 Protect 8

NDC 63002-003 Protect 8

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63002-003?
  4. Protect 8 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:
63002-003
Proprietary Name:
Protect 8
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Advanced Hygienics Llc
Labeler Code:
63002
Product Label ID:
924afbb0-0d3a-4d62-abbd-7cc1f88ddd92
Start Marketing Date: [9]
05-15-2017
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 63002-003-33

Package Description: 9.76 mL in 1 BOTTLE, SPRAY

NDC Code 63002-003-50

Package Description: 500 mL in 1 BOTTLE

NDC Code 63002-003-95

Package Description: 950 mL in 1 BAG

NDC Code 63002-003-99

Package Description: 50 mL in 1 BOTTLE

Product Details

What is NDC 63002-003?

The NDC code 63002-003 is assigned by the FDA to the product Protect 8 which is product labeled by Advanced Hygienics Llc. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 63002-003-33 9.76 ml in 1 bottle, spray , 63002-003-50 500 ml in 1 bottle , 63002-003-95 950 ml in 1 bag , 63002-003-99 50 ml in 1 bottle . 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 Protect 8?

UsesFor hand sanitizing to decrease bacteria on the skin.Recommended for repeated use.

Which are Protect 8 UNII Codes?

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

Which are Protect 8 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 Protect 8?

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".