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  4. NDC Product Code: 61787-442 Zostrix Original Strength

NDC 61787-442 Zostrix Original Strength

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 61787-442?
  4. Zostrix Original Strength Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
61787-442
Proprietary Name:
Zostrix Original Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Akorn Consumer Health
Labeler Code:
61787
Product Label ID:
0eb78397-d6a1-4086-9d6c-02b45b3b9424
Start Marketing Date: [9]
01-09-2006
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61787-442-02

Package Description: 1 TUBE in 1 CARTON / 56.6 g in 1 TUBE

Product Details

What is NDC 61787-442?

The NDC code 61787-442 is assigned by the FDA to the product Zostrix Original Strength which is product labeled by Akorn Consumer Health. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61787-442-02 1 tube in 1 carton / 56.6 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 Zostrix Original Strength?

•for persons under 18 years of age, ask a doctor before using•apply a thin film of cream and gently rub in until fully absorbed•for optimum relief, apply 3 to 4 times daily•best results typically occur after 2 to 4 weeks of continuous use•unless treating hands, wash hands thoroughly with soap and water immediately after use•see package insert for more information

Which are Zostrix Original Strength UNII Codes?

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

Which are Zostrix Original Strength 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.

Patient Education

Capsaicin Topical


Topical capsaicin is used to relieve minor pain in muscles and joints caused by arthritis, backaches, muscle strains, bruises, cramps, and sprains. Capsaicin is a substance that is found in chili peppers. It works by affecting nerve cells in the skin that are associated with pain, which results in decreased activity of these nerve cells and a reduced sense of pain.
[Learn More]


* 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".