NDC 0713-0268 Triple Antibiotic Ointment

NDC Product Code 0713-0268

NDC CODE: 0713-0268

Proprietary Name: Triple Antibiotic Ointment 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

  • 0713 - G&w Laboratories, Inc.

NDC 0713-0268-31

Package Description: 28.4 g in 1 TUBE

Price per Unit: $0.08914 per GM

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

NDC Product Information

Triple Antibiotic Ointment with NDC 0713-0268 is a product labeled by G&w Laboratories, 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: 204602.

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.


Product Labeler Information

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

Labeler Name: G&w Laboratories, Inc.
Labeler Code: 0713
Start Marketing Date: 01-11-1995 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: 12-31-2018 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".

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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]

* Please review the disclaimer below.

Triple Antibiotic Ointment Product Label Images

Triple Antibiotic Ointment 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 Ingredient (In Each Gram)

Bacitracin zinc 400 units Neomycin 3.5 mg Polymyxin B sulfate 5,000 units


First aid antibiotic


First aid to help prevent infection in minor • cuts • scrapes • burns


For external use onlyDo not use• if you are allergic to any of the ingredients • in the eyes• over large areas of the body • longer than 1 week unless directed by a doctorAsk a doctor before use if you have • deep or puncture wounds • animal bites • serious burnsStop use and ask a doctor if  • the condition persists or gets worse• a 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.


• clean the affected area• apply 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 daily• may be covered with a sterile bandage

Other Information

Store at room temperature

Inactive Ingredient

Light mineral oil, white petrolatum

* Please review the disclaimer below.