NDC 69898-501 Premium Hand Sanitizer

Table of Contents

    1. Product Information
    2. Product Packages
    3. What is NDC 69898-501?
    4. Premium Hand Sanitizer Uses
    5. Active Ingredients UNII Codes
    6. Inactive Ingredients UNII Codes
    7. NDC to RxNorm Crosswalk

Product Information

NDC Product Code69898-501
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.		Premium Hand Sanitizer
NDC Directory StatusINACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Md Science Lab Llc
Labeler Code69898
SPL SET ID:002affb4-0499-4c16-bd7f-cff06e9d4e8b
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		04-05-2020
Listing Expiration Date 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.		12-31-2021
Exclude Flag 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". 		I
NDC Code Structure

Product Packages

NDC Code 69898-501-01

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC Code 69898-501-07

Package Description: 221 mL in 1 BOTTLE, PLASTIC

NDC Code 69898-501-08

Package Description: 236 mL in 1 BOTTLE, PLASTIC

NDC Code 69898-501-12

Package Description: 354 mL in 1 BOTTLE, PLASTIC

NDC Code 69898-501-32

Package Description: 946 mL in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

What is NDC 69898-501?

The NDC code 69898-501 is assigned by the FDA to the product Premium Hand Sanitizer which is product labeled by Md Science Lab Llc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 69898-501-01 3785 ml in 1 bottle, plastic , 69898-501-07 221 ml in 1 bottle, plastic , 69898-501-08 236 ml in 1 bottle, plastic , 69898-501-12 354 ml in 1 bottle, plastic , 69898-501-32 946 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 Premium Hand Sanitizer?

Pump a small amount of liquid into palm of hand.Rub thoroughly over all surfaces of both hands.Rub hands together briskly until dry.

Which are Premium Hand Sanitizer UNII Codes?

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

Which are Premium Hand Sanitizer 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 Premium 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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