NDC 67510-0670 Triple Antibiotic Plus Pain Relief

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:
67510-0670
Proprietary Name:
Triple Antibiotic Plus Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kareway Product, Inc.
Labeler Code:
67510
Start Marketing Date: [9]
09-12-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 67510-0670-1

Package Description: 1 TUBE in 1 CARTON / 28.3 g in 1 TUBE

NDC Code 67510-0670-3

Package Description: 1 TUBE in 1 CARTON / 9.4 g in 1 TUBE

NDC Code 67510-0670-5

Package Description: 1 TUBE in 1 CARTON / 14 g in 1 TUBE

Product Details

What is NDC 67510-0670?

The NDC code 67510-0670 is assigned by the FDA to the product Triple Antibiotic Plus Pain Relief which is product labeled by Kareway Product, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 67510-0670-1 1 tube in 1 carton / 28.3 g in 1 tube, 67510-0670-3 1 tube in 1 carton / 9.4 g in 1 tube, 67510-0670-5 1 tube in 1 carton / 14 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 Triple Antibiotic Plus Pain Relief?

Adults and children 2 years of age and older:clean 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 covered with a sterile bandagechildren under 2 years of age: consult a physician

Which are Triple Antibiotic Plus Pain Relief UNII Codes?

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

Which are Triple Antibiotic Plus Pain Relief 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 Triple Antibiotic Plus Pain Relief?

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: 1359350 - bacitracin 500 UNT / neomycin 3.5 MG / polymyxin B 10,000 UNT / pramoxine HCl 10 MG per GM Topical Ointment
  • RxCUI: 1359350 - bacitracin 0.5 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 10 UNT/MG / pramoxine hydrochloride 0.01 MG/MG 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".