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  4. NDC Product Code: 82160-252 Aquax Repellent

NDC 82160-252 Aquax Repellent

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82160-252?
  4. Aquax Repellent 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:
82160-252
Proprietary Name:
Aquax Repellent
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pella Pharmaceuticals Co. Ltd
Labeler Code:
82160
Product Label ID:
d19aeb75-ce56-33ba-e053-2a95a90a5754
Start Marketing Date: [9]
10-04-2010
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 82160-252?

The NDC code 82160-252 is assigned by the FDA to the product Aquax Repellent which is product labeled by Pella Pharmaceuticals Co. Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82160-252-01 1 tube in 1 carton / 75 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 Aquax Repellent?

Aquax ® Repellent Cream hydrates the skin, decreases itchy sensation and provides the feeling of comfort. It's characterized by the presence of the active ingredient Ethyl Butylacetylaminopropionate (IR3535) that acts as a bio-pesticide, its efficacy as insect repellent endures for 6 hours long.

Which are Aquax Repellent UNII Codes?

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

  • ETHYL BUTYLACETYLAMINOPROPIONATE (UNII: 65GQA237EH)
  • ETHYL BUTYLACETYLAMINOPROPIONATE (UNII: 65GQA237EH) (Active Moiety)

Which are Aquax Repellent 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".