NDC 50865-207 Foaming Instant Hand Sanitizer With Aloe And Vitamin E

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:
50865-207
Proprietary Name:
Foaming Instant Hand Sanitizer With Aloe And Vitamin E
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kutol Products Company, Inc.
Labeler Code:
50865
Start Marketing Date: [9]
05-31-2016
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 50865-207-03

Package Description: 208175 mL in 1 DRUM

NDC Code 50865-207-09

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC Code 50865-207-17

Package Description: 50 mL in 1 BOTTLE, PLASTIC

NDC Code 50865-207-24

Package Description: 1000 mL in 1 BAG

NDC Code 50865-207-31

Package Description: 1000 mL in 1 BAG

NDC Code 50865-207-41

Package Description: 1000 mL in 1 BAG

NDC Code 50865-207-78

Package Description: 950 mL in 1 BOTTLE, PLASTIC

NDC Code 50865-207-91

Package Description: 532 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 50865-207?

The NDC code 50865-207 is assigned by the FDA to the product Foaming Instant Hand Sanitizer With Aloe And Vitamin E which is product labeled by Kutol Products Company, Inc.. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 50865-207-03 208175 ml in 1 drum , 50865-207-09 3785 ml in 1 bottle, plastic , 50865-207-17 50 ml in 1 bottle, plastic , 50865-207-24 1000 ml in 1 bag , 50865-207-31 1000 ml in 1 bag , 50865-207-41 1000 ml in 1 bag , 50865-207-78 950 ml in 1 bottle, plastic , 50865-207-91 532 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 Foaming Instant Hand Sanitizer With Aloe And Vitamin E?

Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.Avoid contact with eyes. If contact occurs, flush with water.Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician.Keep out of reach of children. If swallowed, contact a physician or poison control center.

Which are Foaming Instant Hand Sanitizer With Aloe And Vitamin E UNII Codes?

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

Which are Foaming Instant Hand Sanitizer With Aloe And Vitamin E 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 Foaming Instant Hand Sanitizer With Aloe And Vitamin E?

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".