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  4. NDC Product Code: 65113-2428 Gorilla Warfare

NDC 65113-2428 Gorilla Warfare

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 65113-2428?
  5. Gorilla Warfare Uses
  6. Active Ingredients UNII Codes
  7. 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:
65113-2428
Proprietary Name:
Gorilla Warfare
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
G.s. Cosmeceutical Usa, Inc.
Labeler Code:
65113
Product Label ID:
b4b5cd0b-47cf-4601-96ec-df9f98344a73
Start Marketing Date: [9]
04-30-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - PALE TO LIGHT YELLOW)

Code Structure Chart

Product Details

What is NDC 65113-2428?

The NDC code 65113-2428 is assigned by the FDA to the product Gorilla Warfare which is product labeled by G.s. Cosmeceutical Usa, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65113-2428-2 90 ml in 1 bottle, with applicator . 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 Gorilla Warfare?

Shake well. Apply to underarms.

Which are Gorilla Warfare UNII Codes?

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

  • ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE)
  • ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (Active Moiety)

Which are Gorilla Warfare 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:

* Please review the disclaimer below.

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".