NDC 67510-0670 Triple Antibiotic Plus Pain Relief

NDC Product Code 67510-0670

NDC CODE: 67510-0670

Proprietary Name: Triple Antibiotic Plus Pain Relief What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

NDC 67510-0670-1

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

NDC 67510-0670-3

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

NDC 67510-0670-5

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

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Triple Antibiotic Plus Pain Relief with NDC 67510-0670 is a product labeled by Kareway Product, Inc.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1359350.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • PETROLATUM (UNII: 4T6H12BN9U)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Kareway Product, Inc.
Labeler Code: 67510
Start Marketing Date: 09-12-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Information for Patients

Neomycin, Polymyxin, and Bacitracin Topical

Neomycin, Polymyxin, and Bacitracin Topical is pronounced as (nee oh mye' sin) (pol i mix' in) (bass i tray' sin)

Why is neomycin, polymyxin, and bacitracin topical medication prescribed?
Neomycin, polymyxin, and bacitracin combination is used to prevent minor skin injuries such as cuts, scrapes, and burns from becoming infected. Neomycin, polymyxin, and b...
[Read More]
Pramoxine

Pramoxine is pronounced as (pra mox' een)
Why is pramoxine medication prescribed?
Pramoxine is used to temporarily relieve pain and itching from insect bites; poison ivy, poison oak, or poison sumac; minor cuts, scrapes, or burns; minor skin irritation...
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* Please review the disclaimer below.

Triple Antibiotic Plus Pain Relief Product Label Images

Triple Antibiotic Plus Pain Relief Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients (In Each Gram)

Bacitracin Zinc 500 unitsNeomycin 3.5mgPolymyxin B Sulfate 10,000 unitsPramoxine HCl 10mg

Otc - Purpose

Active ingredients(each gram contains)PurposeBacitracin zinc 500 unitsFirst aid antibioticNeomycin sulfate 3.5 mgFirst aid antibioticPolymyxin B sulfate 10,000 unitsFirst aid antibioticPramoxine HCI 10 mgExternal analgesic

Uses

  • First aid to help prevent infection and provide temporary relief of pain or discomfort in minorcutsscrapesburns

Warnings

For external use only

Do Not Use

  • If you are allergic to any of the ingredientsin the eyesover large areas of the body

Ask A Doctor Before Use If You Have

  • Ask a doctor before use if you havedeep or puncture woundsanimal bitesserious burns

Stop Use And Ask A Doctor If

  • You need to use longer than 1 weekcondition persists or gets worsecondition persists for more than 1 week, or clear up and occur again within a few daysa rash or other allergic reaction develops

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • 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

Other Information

Store at 20°-25°C (68°-77°F)

Purpose

First aid antibioticFirst aid antibioticFirst aid antibioticExternal analgesic

Inactive Ingredients

White petrolatum

* Please review the disclaimer below.