NDC 74621-026 Joby Instant Hand Sanitrizer

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:
74621-026
Proprietary Name:
Joby Instant Hand Sanitrizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
74621
Start Marketing Date: [9]
05-20-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 74621-026?

The NDC code 74621-026 is assigned by the FDA to the product Joby Instant Hand Sanitrizer which is product labeled by Aogrand International Trade Corporation. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 74621-026-01 500 ml in 1 bottle, plastic , 74621-026-02 1000 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 Joby Instant Hand Sanitrizer?

Place enough product into your palms and thoroughly spread on both hands.rub into skin until dry.Other informationstore below 110 ℉ (43 ℃ ). may discolor certain fabrics or surfaces.

Which are Joby Instant Hand Sanitrizer UNII Codes?

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

Which are Joby Instant Hand Sanitrizer 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 Joby Instant Hand Sanitrizer?

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".