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  4. NDC Product Code: 64646-328 Servclean Gel Hand Sanitizer

NDC 64646-328 Servclean Gel Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64646-328?
  4. Servclean Gel Hand Sanitizer 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:
64646-328
Proprietary Name:
Servclean Gel Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Charlotte Products Ltd
Labeler Code:
64646
Product Label ID:
a67b3c1c-c221-4b25-e053-2a95a90a3d0b
Start Marketing Date: [9]
05-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 64646-328-02

Package Description: 2000 mL in 1 BOTTLE, PLASTIC

NDC Code 64646-328-03

Package Description: 3600 mL in 1 BOTTLE, PLASTIC

NDC Code 64646-328-04

Package Description: 3780 mL in 1 BOTTLE, PLASTIC

NDC Code 64646-328-07

Package Description: 700 mL in 1 BOTTLE, PLASTIC

NDC Code 64646-328-12

Package Description: 500 mL in 1 BOTTLE, PLASTIC

NDC Code 64646-328-19

Package Description: 1890 mL in 1 BOTTLE, PLASTIC

NDC Code 64646-328-20

Package Description: 18900 mL in 1 PAIL

NDC Code 64646-328-21

Package Description: 208000 mL in 1 DRUM

NDC Code 64646-328-22

Package Description: 1000000 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK

NDC Code 64646-328-25

Package Description: 225 mL in 1 BOTTLE, PLASTIC

NDC Code 64646-328-60

Package Description: 60 mL in 1 BOTTLE, PLASTIC

NDC Code 64646-328-70

Package Description: 100 mL in 1 BOTTLE, PLASTIC

NDC Code 64646-328-75

Package Description: 750 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 64646-328?

The NDC code 64646-328 is assigned by the FDA to the product Servclean Gel Hand Sanitizer which is product labeled by Charlotte Products Ltd. The product's dosage form is . The product is distributed in 13 packages with assigned NDC codes 64646-328-02 2000 ml in 1 bottle, plastic , 64646-328-03 3600 ml in 1 bottle, plastic , 64646-328-04 3780 ml in 1 bottle, plastic , 64646-328-07 700 ml in 1 bottle, plastic , 64646-328-12 500 ml in 1 bottle, plastic , 64646-328-19 1890 ml in 1 bottle, plastic , 64646-328-20 18900 ml in 1 pail , 64646-328-21 208000 ml in 1 drum , 64646-328-22 1000000 ml in 1 container, flexible intermediate bulk , 64646-328-25 225 ml in 1 bottle, plastic , 64646-328-60 60 ml in 1 bottle, plastic , 64646-328-70 100 ml in 1 bottle, plastic , 64646-328-75 750 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 Servclean Gel Hand Sanitizer?

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 Servclean Gel Hand Sanitizer UNII Codes?

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

Which are Servclean Gel 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:

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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".