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  4. NDC Product Code: 11697-318 Forever Hand Sanitizer Hand Sanitizer

NDC 11697-318 Forever Hand Sanitizer Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11697-318?
  4. Forever Hand Sanitizer 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:
11697-318
Proprietary Name:
Forever Hand Sanitizer Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aloe Vera Of America, Inc.
Labeler Code:
11697
Product Label ID:
296bea0a-c91c-28a4-e054-00144ff8d46c
Start Marketing Date: [9]
08-16-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 11697-318-02

Package Description: 59 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 11697-318?

The NDC code 11697-318 is assigned by the FDA to the product Forever Hand Sanitizer Hand Sanitizer which is product labeled by Aloe Vera Of America, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11697-318-02 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 Forever Hand Sanitizer Hand Sanitizer?

Do not use in or near the eyes. If contact occurs, rinse throughly with water.avoid contact with broken skin.

Which are Forever Hand Sanitizer Hand Sanitizer UNII Codes?

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

Which are Forever Hand Sanitizer 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".