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  4. NDC Product Code: 42333-100 Borasol

NDC 42333-100 Borasol

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 42333-100?
  4. Borasol Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
42333-100
Proprietary Name:
Borasol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Laboratorios Dr. Collado, C X A.
Labeler Code:
42333
Product Label ID:
140c61a9-a4a9-4669-8a58-af9265a8c3e4
Start Marketing Date: [9]
01-01-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 42333-100?

The NDC code 42333-100 is assigned by the FDA to the product Borasol which is product labeled by Laboratorios Dr. Collado, C X A.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42333-100-04 1 jar in 1 box / 114 g in 1 jar. 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 Borasol?

Uses:First aid to help prevent infection in minor cuts, scrapes, and burns. For the temporary relief of pain and itching due to minor burns, sunburns, minor cuts, abrasions, insect bites and minor skin irritations.

Which are Borasol UNII Codes?

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

Which are Borasol 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 Borasol?

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:
  • RxCUI: 1424242 - eucalyptol 0.091 % / menthol 0.01 % / methyl salicylate 0.055 % / thymol 0.063 % Topical Powder
  • RxCUI: 1424242 - eucalyptol 0.0091 MG/MG / menthol 0.0001 MG/MG / methyl salicylate 0.0055 MG/MG / thymol 0.0063 MG/MG Topical Powder

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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".