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  4. NDC Product Code: 73945-003 Premier Pure Protection

NDC 73945-003 Premier Pure Protection

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73945-003?
  4. Premier Pure Protection 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:
73945-003
Proprietary Name:
Premier Pure Protection
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rpp Products, Inc.
Labeler Code:
73945
Product Label ID:
2e2b3a15-4caa-42a1-a5ae-61ca4d941713
Start Marketing Date: [9]
04-10-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73945-003-01

Package Description: 59 mL in 1 BOTTLE, PLASTIC

NDC Code 73945-003-02

Package Description: 88.72 mL in 1 BOTTLE, PLASTIC

NDC Code 73945-003-03

Package Description: 118.3 mL in 1 BOTTLE, PLASTIC

NDC Code 73945-003-04

Package Description: 236.59 mL in 1 BOTTLE, PLASTIC

NDC Code 73945-003-05

Package Description: 295.74 mL in 1 BOTTLE, PLASTIC

NDC Code 73945-003-06

Package Description: 443.6 mL in 1 BOTTLE, PLASTIC

NDC Code 73945-003-07

Package Description: 473 mL in 1 BOTTLE, PLASTIC

NDC Code 73945-003-08

Package Description: 946 mL in 1 BOTTLE, PLASTIC

NDC Code 73945-003-09

Package Description: 1890 mL in 1 BOTTLE, PLASTIC

NDC Code 73945-003-10

Package Description: 2000 mL in 1 BOTTLE, PLASTIC

NDC Code 73945-003-11

Package Description: 2800 mL in 1 BOTTLE, PLASTIC

NDC Code 73945-003-12

Package Description: 3780 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 73945-003?

The NDC code 73945-003 is assigned by the FDA to the product Premier Pure Protection which is product labeled by Rpp Products, Inc.. The product's dosage form is . The product is distributed in 12 packages with assigned NDC codes 73945-003-01 59 ml in 1 bottle, plastic , 73945-003-02 88.72 ml in 1 bottle, plastic , 73945-003-03 118.3 ml in 1 bottle, plastic , 73945-003-04 236.59 ml in 1 bottle, plastic , 73945-003-05 295.74 ml in 1 bottle, plastic , 73945-003-06 443.6 ml in 1 bottle, plastic , 73945-003-07 473 ml in 1 bottle, plastic , 73945-003-08 946 ml in 1 bottle, plastic , 73945-003-09 1890 ml in 1 bottle, plastic , 73945-003-10 2000 ml in 1 bottle, plastic , 73945-003-11 2800 ml in 1 bottle, plastic , 73945-003-12 3780 ml in 1 bottle, plastic . 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 Premier Pure Protection?

Put enough product in your palm to cover hands and rub hands together briskly until dry.children under 6 years of age should be supervised when using this PREMIER PURE

Which are Premier Pure Protection UNII Codes?

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

Which are Premier Pure Protection 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 Premier Pure Protection?

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".