NDC 50563-109 Ocean Mist Scented Hand Sanitizer Anti-bacterial

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:
50563-109
Proprietary Name:
Ocean Mist Scented Hand Sanitizer Anti-bacterial
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Enchante Accessories Inc.
Labeler Code:
50563
Start Marketing Date: [9]
06-18-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50563-109-01

Package Description: 236 mL in 1 BOTTLE

Product Details

What is NDC 50563-109?

The NDC code 50563-109 is assigned by the FDA to the product Ocean Mist Scented Hand Sanitizer Anti-bacterial which is product labeled by Enchante Accessories Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50563-109-01 236 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 Ocean Mist Scented Hand Sanitizer Anti-bacterial?

UsesTo decrease bacteria on the skin that could cause diseasesRecommended for repeated use

Which are Ocean Mist Scented Hand Sanitizer Anti-bacterial UNII Codes?

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

Which are Ocean Mist Scented Hand Sanitizer Anti-bacterial 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 Ocean Mist Scented Hand Sanitizer Anti-bacterial?

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".