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  4. NDC Product Code: 69020-210 Makesense First Aid

NDC 69020-210 Makesense First Aid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69020-210?
  4. Makesense First Aid 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:
69020-210
Proprietary Name:
Makesense First Aid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cherry Hill Sales Co
Labeler Code:
69020
Product Label ID:
9b4666e0-d7c8-4b50-aa0c-c6a7b8e52617
Start Marketing Date: [9]
07-31-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 69020-210?

The NDC code 69020-210 is assigned by the FDA to the product Makesense First Aid which is product labeled by Cherry Hill Sales Co. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69020-210-28 28 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 Makesense First Aid?

■ Cleanse affected area ■ Apply a small amount of this product (an amount equal to the surface of a finger) on the area 1 to 3 times daily

Which are Makesense First Aid UNII Codes?

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

Which are Makesense First Aid 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 Makesense First Aid?

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: 1426594 - lidocaine HCl 0.5 % / phenol 0.5 % Topical Cream
  • RxCUI: 1426594 - lidocaine hydrochloride 5 MG/ML / phenol 5 MG/ML Topical Cream
  • RxCUI: 1426594 - lidocaine hydrochloride 0.5 % / phenol 0.5 % Topical Cream

* 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".