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  4. NDC Product Code: 75462-888 Liquid Hand Cleanser

NDC 75462-888 Liquid Hand Cleanser

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75462-888?
  4. Liquid Hand Cleanser 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:
75462-888
Proprietary Name:
Liquid Hand Cleanser
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sandy Maine Inc.
Labeler Code:
75462
Product Label ID:
a2cf8d7e-d587-5180-e053-2995a90a9ef5
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 75462-888?

The NDC code 75462-888 is assigned by the FDA to the product Liquid Hand Cleanser which is product labeled by Sandy Maine Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 75462-888-01 54 ml in 1 bottle, glass , 75462-888-03 236 ml in 1 bottle, plastic , 75462-888-04 111 ml in 1 bottle, glass . 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 Liquid Hand Cleanser?

Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Liquid Hand Cleanser UNII Codes?

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

Which are Liquid Hand Cleanser 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".