NDC 78026-015 Instant Hand Sanitizer

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:
78026-015
Proprietary Name:
Instant Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
78026
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 78026-015?

The NDC code 78026-015 is assigned by the FDA to the product Instant Hand Sanitizer which is product labeled by Yangzhou Olande Cosmetic Co., Ltd.. The product's dosage form is . The product is distributed in 14 packages with assigned NDC codes 78026-015-01 30 ml in 1 bottle , 78026-015-02 40 ml in 1 bottle , 78026-015-03 50 ml in 1 bottle , 78026-015-04 55 ml in 1 bottle , 78026-015-05 60 ml in 1 bottle , 78026-015-06 80 ml in 1 bottle , 78026-015-07 100 ml in 1 bottle , 78026-015-08 120 ml in 1 bottle , 78026-015-09 200 ml in 1 bottle , 78026-015-10 236 ml in 1 bottle , 78026-015-11 300 ml in 1 bottle , 78026-015-12 500 ml in 1 bottle , 78026-015-13 1000 ml in 1 bottle , 78026-015-14 5000 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 Instant Hand Sanitizer?

Place enough product on hands to cover all surfaces. Rub hands together until dry. Use as needed no need to rinse with water. For children under 6 years of age, use only under adult supervision. Not recommender for infants.

What is the NDC to RxNorm Crosswalk for Instant Hand Sanitizer?

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".