NDC 0363-2016 Walgreens Triple Antibiotic

NDC Product Code 0363-2016

NDC CODE: 0363-2016

Proprietary Name: Walgreens Triple 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

  • 0363 - Walgreen Company

NDC 0363-2016-03

Package Description: 1 TUBE in 1 CARTON > 60 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

Walgreens Triple Antibiotic with NDC 0363-2016 is a product labeled by Walgreen Company. 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.

  • 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: Walgreen Company
Labeler Code: 0363
Start Marketing Date: 12-14-1995 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: 12-31-2019 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

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Why is neomycin, polymyxin, and bacitracin topical medication prescribed?
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Walgreens Triple Antibiotic Product Label Images

Walgreens Triple 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

Other

Drug Facts

DISTRIBUTED BY: WALGREEN CO.200 WILMOT RD., DEERFIELD, IL 60015

Otc - Purpose

Active ingredients (each gram contains)PurposeBacitracin zinc 400 unitsFirst aid antibioticNeomycin sulfate 3.5 mgFirst aid antibioticPolymyxin B sulfate 5,000 unitsFirst aid antibiotic

Uses

  • First aid to help prevent infection in minor:cutsscrapesburns

Warnings

For external use only.

Do Not Use

  • In the eyesover large areas of the bodyif you are allergic to any of the ingredients

Ask A Doctor Before Use If You Have

  • Deep or puncture woundsanimal bitesserious burns

Stop Use And Ask A Doctor If

  • Condition persists or gets worseyou need to use longer than 1 weeka 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.

Directions

  • Clean the affected area and dry thoroughlyapply 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 bandage

Other Information

  • To open: unscrew cap, pull tab to remove foil sealstore at 20° to 25°C (68° to 77°F)see carton or tube crimp for lot number and expiration date

Inactive Ingredient

White petrolatum

Questions?

Call 1-866-923-4914

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