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  4. NDC Product Code: 83004-020 Terramed Just Think Comfort Jock Itch Antifungal Treatment

NDC 83004-020 Terramed Just Think Comfort Jock Itch Antifungal Treatment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83004-020?
  4. Terramed Just Think Comfort Jock Itch Antifungal Treatment Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk
  8. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Get all the details for National Drug Code (NDC) 83004-020 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
83004-020
Proprietary Name:
Terramed Just Think Comfort Jock Itch Antifungal Treatment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rida Llc
Labeler Code:
83004
Product Label ID:
2acb9027-8f20-4b77-9b45-17fe11622c7c
FDA Application Number: [6]
M005
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
03-01-2025
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
I
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Product Details

What is NDC 83004-020?

The NDC code 83004-020 is assigned by the FDA to the product Terramed Just Think Comfort Jock Itch Antifungal Treatment which is product labeled by Rida Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 83004-020-01 1 bottle, spray in 1 box / 120 ml in 1 bottle, spray. 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 Terramed Just Think Comfort Jock Itch Antifungal Treatment?

Adults and children 12 years and over:wash affected area and dry thoroughlyshake can well and spray a thin layer over affected area twice daily (morning andnight) supervise children in the use of this productuse daily for 2 weeksif condition persists longer, ask a doctorthis product is not effective on the scalp or nailswash hands after each usein case of clogging, clean with a pin Children under 12 years: ask a doctor 

Which are Terramed Just Think Comfort Jock Itch Antifungal Treatment UNII Codes?

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

Which are Terramed Just Think Comfort Jock Itch Antifungal Treatment 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:

What is the NDC to RxNorm Crosswalk for Terramed Just Think Comfort Jock Itch Antifungal Treatment?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Patient Education

Miconazole Topical


Topical miconazole is used to treat tinea corporis(ringworm; fungal skin infection that causes a red scaly rash on different parts of the body), tinea cruris (jock itch; fungal infection of the skin in the groin or buttocks), and tinea pedis (athlete's foot; fungal infection of the skin on the feet and between the toes). Miconazole is in a class of antifungal medications called imidazoles. It works by stopping the growth of fungi that cause infection. Not all products should be used to treat all of these conditions. Please read the label for each product to select the one to treat your condition.
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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.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".