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  4. NDC Product Code: 26509-0200 Clorox Healthcare Gbg Aloegel Instant Hand Sanitizer

NDC 26509-0200 Clorox Healthcare Gbg Aloegel Instant Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 26509-0200?
  4. Clorox Healthcare Gbg Aloegel Instant 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:
26509-0200
Proprietary Name:
Clorox Healthcare Gbg Aloegel Instant Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Clorox Company
Labeler Code:
26509
Product Label ID:
8d46e2b2-35d8-53d2-e053-2a95a90abdf2
Start Marketing Date: [9]
07-09-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 26509-0200-2

Package Description: 532 mL in 1 BOTTLE

NDC Code 26509-0200-3

Package Description: 800 mL in 1 BAG

Product Details

What is NDC 26509-0200?

The NDC code 26509-0200 is assigned by the FDA to the product Clorox Healthcare Gbg Aloegel Instant Hand Sanitizer which is product labeled by The Clorox Company. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 26509-0200-2 532 ml in 1 bottle , 26509-0200-3 800 ml in 1 bag . 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 Clorox Healthcare Gbg Aloegel Instant Hand Sanitizer?

Apply gel liberally to unsoiled hands and rub thoroughlyallow to dry without wiping or rinsing

Which are Clorox Healthcare Gbg Aloegel Instant Hand Sanitizer UNII Codes?

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

Which are Clorox Healthcare Gbg Aloegel Instant 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".