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  4. NDC Product Code: 41250-607 Crisp Apple Hand Sani

NDC 41250-607 Crisp Apple Hand Sani

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 41250-607?
  4. Crisp Apple Hand Sani Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
41250-607
Proprietary Name:
Crisp Apple Hand Sani
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Meijer Distribution, Inc
Labeler Code:
41250
Product Label ID:
546dd82c-882e-4642-b252-944e191192f2
Start Marketing Date: [9]
03-11-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 41250-607?

The NDC code 41250-607 is assigned by the FDA to the product Crisp Apple Hand Sani which is product labeled by Meijer Distribution, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41250-607-16 59 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 Crisp Apple Hand Sani?

Wet hands thoroughly with product and allow to dry without wipingfor children under 6, use only under adult supervisionnot recommed for infants

Which are Crisp Apple Hand Sani UNII Codes?

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

Which are Crisp Apple Hand Sani 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:

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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".