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  4. NDC Product Code: 78804-213 Cypress Bio-tech Hand Sanitizing Foam

NDC 78804-213 Cypress Bio-tech Hand Sanitizing Foam

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78804-213?
  4. Cypress Bio-tech Hand Sanitizing Foam 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:
78804-213
Proprietary Name:
Cypress Bio-tech Hand Sanitizing Foam
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Allure Chemicals Lp
Labeler Code:
78804
Product Label ID:
30456a24-8467-40a3-89ba-32c25d1eb244
Start Marketing Date: [9]
05-07-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 78804-213-16

Package Description: 500 mL in 1 BOTTLE, PLASTIC

NDC Code 78804-213-50

Package Description: 50 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 78804-213?

The NDC code 78804-213 is assigned by the FDA to the product Cypress Bio-tech Hand Sanitizing Foam which is product labeled by Allure Chemicals Lp. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 78804-213-16 500 ml in 1 bottle, plastic , 78804-213-50 50 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 Cypress Bio-tech Hand Sanitizing Foam?

* Place enough product on hands to cover all surfaces. Rub hands thoroughly with warm water for 30 seconds.* Store between 15-30°C (59-86 °F)* Avoid freezing and excessive heat above 40 °C (104 °F)

Which are Cypress Bio-tech Hand Sanitizing Foam UNII Codes?

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

Which are Cypress Bio-tech Hand Sanitizing Foam 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 Cypress Bio-tech Hand Sanitizing Foam?

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:

* Please review the disclaimer below.

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".