NDC 0924-5603 Triple Antibiotic

NDC Product Code 0924-5603

NDC 0924-5603-02

Package Description: 6 PACKET in 1 BAG > .5 g in 1 PACKET (0924-5603-01)

NDC 0924-5603-03

Package Description: 10 PACKET in 1 BOX > .5 g in 1 PACKET (0924-5603-01)

NDC 0924-5603-04

Package Description: 12 PACKET in 1 BOX > .5 g in 1 PACKET (0924-5603-01) (0924-5603-01)

NDC 0924-5603-05

Package Description: 25 PACKET in 1 BOX > .5 g in 1 PACKET (0924-5603-01) (0924-5603-01)

NDC 0924-5603-06

Package Description: 60 PACKET in 1 BOX > .5 g in 1 PACKET (0924-5603-01) (0924-5603-01)

NDC 0924-5603-07

Package Description: 144 PACKET in 1 BOX > .5 g in 1 PACKET (0924-5603-01) (0924-5603-01)

NDC 0924-5603-08

Package Description: 10 PACKET in 1 BOX > .5 g in 1 PACKET (0924-5603-01)

NDC 0924-5603-09

Package Description: 12 PACKET in 1 BOX > .5 g in 1 PACKET (0924-5603-01)

NDC 0924-5603-10

Package Description: 60 PACKET in 1 BOX > .5 g in 1 PACKET (0924-5603-01)

NDC 0924-5603-11

Package Description: 144 PACKET in 1 BOX > .5 g in 1 PACKET (0924-5603-01)

NDC 0924-5603-12

Package Description: 25 PACKET in 1 BOX > .5 g in 1 PACKET (0924-5603-01)

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

NDC Product Information

Triple Antibiotic with NDC 0924-5603 is a product labeled by Acme United Corporation. The generic name of Triple Antibiotic is . The product's dosage form is and is administered via form.

Labeler Name: Acme United Corporation

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

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: Acme United Corporation
Labeler Code: 0924
Start Marketing Date: 01-27-2012 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: E 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. Values = ‘Y’ or ‘N’.

* 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]

* Please review the disclaimer below.

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

Active Ingredients (In Each Gram)

Bacitracin zinc 400 units
Neomycin sulfate 5 mg (equivalent to 3.5 mg of neomycin base)
Polymyxin-B sulfate 5000 units

Purpose

First Aid Antibiotics

Uses

  • First aid to help prevent infection in
  • Minor cuts
  • Scrapes
  • Burns

Warnings:

For external use only.

Do Not Use

  • In the eyes or apply over large areas of the body
  • If you are allergic to any of the ingredients
  • Longer than 1 week unless directed by a doctor

Ask A Doctor Before Use If You Have

  • Deep or puncture wounds, animal bites, or serious burns

Stop Use And Ask A Doctor If

  • Condition persists or gets worse
  • A rash or other allergic reaction develops

Otc - Keep Out Of Reach Of Children

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

Directions:

  • Clean the affected area
  • Apply a small amount of this product (an amount equal to the surface area of a finger) on the area 1 to 3 times daily
  • May be covered with a sterile bandage

Other Information

  • Store at 15° to 25° C (59° to 77° F)
  • Do not use if packet is open or torn

Inactive Ingredient

Petrolatum

Questions? 1-800-835-2263

Manufactured for:Acme United CorporationFairfield, CT 06824
REORDERwww.PhysiciansCareFirstAid.com1 800 835 2263

* Please review the disclaimer below.