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  4. NDC Product Code: 73769-004 Hand Sanitizer Liquid With Lavender

NDC 73769-004 Hand Sanitizer Liquid With Lavender

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73769-004?
  4. Hand Sanitizer Liquid With Lavender Uses
  5. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
73769-004
Proprietary Name:
Hand Sanitizer Liquid With Lavender
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nature's Fusions, Llc
Labeler Code:
73769
Product Label ID:
a0618307-ad0e-a907-e053-2995a90a4239
Start Marketing Date: [9]
03-16-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 73769-004?

The NDC code 73769-004 is assigned by the FDA to the product Hand Sanitizer Liquid With Lavender which is product labeled by Nature's Fusions, Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 73769-004-08 236 ml in 1 bottle, spray , 73769-004-30 30 ml in 1 bottle, spray , 73769-004-60 59 ml in 1 bottle, spray . 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 Hand Sanitizer Liquid With Lavender?

Place a small amount of product in your palm to thoroughly cover your hands.Rub hands together briskly until dry.Children under 6 years should be supervised when using this product.

What is the NDC to RxNorm Crosswalk for Hand Sanitizer Liquid With Lavender?

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".