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  4. NDC Product Code: 73659-005 Triple Antibiotic

NDC 73659-005 Triple Antibiotic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73659-005?
  4. Triple Antibiotic Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
73659-005
Proprietary Name:
Triple Antibiotic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rapid Care, Inc
Labeler Code:
73659
Product Label ID:
b7120f2c-436d-76b9-e053-2995a90a334c
Start Marketing Date: [9]
04-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73659-005-01

Package Description: .5 g in 1 PACKET

NDC Code 73659-005-10

Package Description: .5 g in 1 PACKET

Product Details

What is NDC 73659-005?

The NDC code 73659-005 is assigned by the FDA to the product Triple Antibiotic which is product labeled by Rapid Care, Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 73659-005-01 .5 g in 1 packet , 73659-005-10 .5 g in 1 packet . 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 Triple Antibiotic?

Clean affected areaapply a small amount 1 to 3 times dailymay cover with a sterile bandage

Which are Triple Antibiotic UNII Codes?

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

Which are Triple Antibiotic 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

[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".