NDC 76286-668 Non-negotiables Fast-acting Sanitizing

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:
76286-668
Proprietary Name:
Non-negotiables Fast-acting Sanitizing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
76286
Start Marketing Date: [9]
04-01-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 76286-668?

The NDC code 76286-668 is assigned by the FDA to the product Non-negotiables Fast-acting Sanitizing which is product labeled by Skinn Cosmetics, Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 76286-668-08 236 ml in 1 bottle , 76286-668-12 355 ml in 1 bottle , 76286-668-13 385 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 Non-negotiables Fast-acting Sanitizing?

Dispense enough sanitizer to cover desired areasRub product into skin until dryChildren under 6 years of age should be supervised when using this product

Which are Non-negotiables Fast-acting Sanitizing UNII Codes?

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

Which are Non-negotiables Fast-acting Sanitizing 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 Non-negotiables Fast-acting Sanitizing?

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".