NDC 68788-9488 Double Antibiotic

NDC Product Code 68788-9488

NDC CODE: 68788-9488

Proprietary Name: Double Antibiotic 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

  • 68788 - Preferred Pharmaceuticals, Inc.

NDC 68788-9488-2

Package Description: 1 TUBE in 1 CARTON > 28.35 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

Double Antibiotic with NDC 68788-9488 is a product labeled by Preferred Pharmaceuticals, 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: 308512.

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: Preferred Pharmaceuticals, Inc.
Labeler Code: 68788
Start Marketing Date: 05-20-2014 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".

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Information for Patients

Bacitracin Ophthalmic

Bacitracin Ophthalmic is pronounced as (bas'' i tray' sin)

Why is bacitracin ophthalmic medication prescribed?
Ophthalmic bacitracin is used to treat bacterial infections of the eye. Bacitracin is in a class of medications called antibiotics. It works by killing bacteria that caus...
[Read More]

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Double Antibiotic Product Label Images

Double Antibiotic 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 (equal to 500 bacitracin units)Polymyxin B Sulfate (equal to 10,000 polymyxin B units)

Purpose

Antibiotic Antibiotic

Uses

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

Otc - Do Not Use

  • Do not use •in the eyes •over large areas of the body •if you are allergic to any of the ingredients

Otc - Ask Doctor

Ask a doctor before use in case of deep or puncture wounds, animal bites or serious burns

Otc - When Using

When using this product do not use longer than 1 week unless directed by a doctor

Otc - Stop Use

  • Stop use and ask a doctor if •the condition persists or gets worse •if a rash or other allergic reaction develops

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

  • Directions •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

Other information store at room temperature

Questions or comments? call toll free 1-800-645-9833

Inactive Ingredient

Inactive ingredient white petrolatum

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