NDC 75983-555 First Aid Research Bacitraycin Plus Maximum Vertical

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
75983-555
Proprietary Name:
First Aid Research Bacitraycin Plus Maximum Vertical
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
75983
Start Marketing Date: [9]
03-06-2014
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 75983-555?

The NDC code 75983-555 is assigned by the FDA to the product First Aid Research Bacitraycin Plus Maximum Vertical which is product labeled by First Aid Research Corp.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75983-555-28 1 tube in 1 box / 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 First Aid Research Bacitraycin Plus Maximum Vertical?

Directionsclean the affected areaapply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times dailymay be convered with a sterile bandage

Which are First Aid Research Bacitraycin Plus Maximum Vertical UNII Codes?

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

Which are First Aid Research Bacitraycin Plus Maximum Vertical 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 First Aid Research Bacitraycin Plus Maximum Vertical?

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: 1490996 - bacitracin 500 UNT per GM / lidocaine HCl 40 MG per GM Topical Ointment
  • RxCUI: 1490996 - bacitracin 0.5 UNT/MG / lidocaine hydrochloride 0.04 MG/MG Topical Ointment
  • RxCUI: 1490996 - bacitracin 500 UNT per GM / lidocaine hydrochloride 40 MG per GM Topical Ointment

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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".