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  4. NDC Product Code: 76555-006 Ec Pure Instant Cream Hand Sanitizer Unscented

NDC 76555-006 Ec Pure Instant Cream Hand Sanitizer Unscented

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76555-006?
  4. Ec Pure Instant Cream Hand Sanitizer Unscented 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:
76555-006
Proprietary Name:
Ec Pure Instant Cream Hand Sanitizer Unscented
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ec Labs Inc.
Labeler Code:
76555
Product Label ID:
ac15d72d-7d5b-4046-e053-2a95a90ada2a
Start Marketing Date: [9]
07-31-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 76555-006?

The NDC code 76555-006 is assigned by the FDA to the product Ec Pure Instant Cream Hand Sanitizer Unscented which is product labeled by Ec Labs Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76555-006-01 60 g in 1 tube . 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 Ec Pure Instant Cream Hand Sanitizer Unscented?

Apply a small amount to hands and spread evenly.Rub thoroughly into hands for at least 30 seconds.Allow to dry.For occasional and personal use.Supervise children under 6 years of age when using this product.

Which are Ec Pure Instant Cream Hand Sanitizer Unscented UNII Codes?

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

Which are Ec Pure Instant Cream Hand Sanitizer Unscented 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:

  • GLYCERIN (UNII: PDC6A3C0OX)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • WATER (UNII: 059QF0KO0R)
  • PEG/PPG-18/12 DIMETHICONE (UNII: 2AY8NFX9E4)
  • AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
  • CYCLOMETHICONE (UNII: NMQ347994Z)
  • SODIUM ACRYLOYLDIMETHYLTAURATE (UNII: 2T9Q6EKI0G)

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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".