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  4. NDC Product Code: 50138-018 Iodine

NDC 50138-018 Iodine

Solution, Concentrate - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50138-018?
  4. Iodine Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Get all the details for National Drug Code (NDC) 50138-018 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:
50138-018
Proprietary Name:
Iodine
Non-Proprietary Name: [1]
Iodine
Substance Name: [2]
Iodine
NDC Directory Status:
Bulk Ingredient - Animal Drug
Product Type: [3]
UNFINISHED PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution, Concentrate - A liquid preparation (i.e., a substance that flows readily in its natural state) that contains a drug dissolved in a suitable solvent or mixture of mutually miscible solvents; the drug has been strengthened by the evaporation of its nonactive parts.
Labeler Name: [5]
Ecolab Inc.
Labeler Code:
50138
Product Label ID:
412bdb75-ac3b-4557-ac94-dda28575fe12
Marketing Category: [8]
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date: [9]
11-15-2019
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Unfinished Product: [13]
Yes
Code Navigator:

Code Structure Chart

Product Details

What is NDC 50138-018?

The NDC code 50138-018 is assigned by the FDA to the UNFINISHED product Iodine which is bulk ingredient - animal drug product labeled by Ecolab Inc.. The generic name of Iodine is iodine. The product's dosage form is solution, concentrate. The product is distributed in 4 packages with assigned NDC codes 50138-018-17 56800 ml in 1 drum , 50138-018-21 208000 ml in 1 drum , 50138-018-35 2000000 ml in 1 container , 50138-018-44 1134000 ml in 1 container . 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 Iodine?

DIRECTIONS:ECO-DINE CONCENTRATE MUST BE DILUTED BEFORE USEDO NOT MIX WITH ANYTHING BUT COOL, POTABLE WATERFOR USE ONLY IN A DISPENSING SYSTEM RECOMMENDED BY ECOLAB Dilution Parameter(s):IMPORTANT: Never use concentrated product on teats.  Once concentrated teat dip product has been properly diluted, do not further dilute with water or mix with any other teat dips.  If product in dip cup becomes visibly dirty, discard contents and replenish with fresh product.  Do not reuse or return any unused product to the original container.Udder Prep:  When using an udder wash step before milking, make sure to wash teats with appropriate udder wash solution using proper cleaning procedures.  Teats should then be dried with single-service towels.Application of Diluted Eco-Dine ConcentrateDirections for Teat DippingPre-Milk Dipping:  Before each cow is milked, and using fresh final RTU product dip each teat full-length into the teat dip cup.  Wipe teats after dipping using single-service towels to avoid contamination of milk.Post-Milk Dipping: Using fresh final RTU product dip each teat full-length into the teat dip cup.  Do not wipe. Allow to air dry.  Do not turn cows out in freezing weather until the product is completely dry.Directions for Teat SprayingPre-Milk Spraying: Before each cow is milked, and using fresh final RTU product spray entire teat.  Wipe teats after dipping using single-service towels to avoid contamination of milk.Post-Milk Spraying: Using fresh final RTU product spray entire teat immediately after each milking.  Do not wipe. Allow to air dry.  Do not turn cows out in freezing weather until the product is completely dry.Expanded Usage: When freshening cows, begin dipping teats twice daily for about 10 days before calving.PRECAUTION: Eco-Dine Concentrate is not intended to cure or help the healing of chapped or irritated teats.  As with any germicide, irritation or sensitization may occur in sensitive animals.  In case of teat irritation or chapping, have the condition examined and, if necessary, treated by a veterinarian.Consult your Ecolab representative for specific use instructions and recommended dispensing equipment.

What are Iodine Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • IODINE 40 mg/mL - A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.

Which are Iodine UNII Codes?

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

Which are Iodine 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

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[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".

[13] What is an Unfinished Product? - This field indicates if the product is an unfinished drug. An unfinished drug is an active pharmaceutical ingredient either alone or with other ingredients that is not a finished drug product. Unfinished drugs are used to process other drugs or for drug compounding.