NDC 80622-555 Careful Hand Sanitizer Orange

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
Proprietary Name:
Careful Hand Sanitizer Orange
Product Type: [3]
Labeler Name: [5]
Brainstem Innovations Co.
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Structure:
Code Navigator:

Product Characteristics

ORANGE (C73406)

Product Packages

NDC Code 80622-555-12

Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 100 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 80622-555?

The NDC code 80622-555 is assigned by the FDA to the product Careful Hand Sanitizer Orange which is product labeled by Brainstem Innovations Co.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80622-555-12 1 bottle, spray in 1 carton / 100 ml in 1 bottle, spray. 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 Careful Hand Sanitizer Orange?

• wet hands thoroughly with product • allow to dry without wiping • supervise children under 6 years old • not recommended for infants

Which are Careful Hand Sanitizer Orange UNII Codes?

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

Which are Careful Hand Sanitizer Orange 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 Careful Hand Sanitizer Orange?

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".