Triple Antibiotic Ointment
FDA Label NDC 11673-892

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Triple Antibiotic (NDC 11673-892). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding drug facts, active ingredients, purpose, uses, warnings, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredients

Bacitracin 400

Neomycin 3.5 mg

Polymyxin B 5,000 units

Purpose

First aid antibiotic

First aid antibiotic

First aid antibiotic

Uses

First aid to help prevent infection in minor:

  • cuts
  • scrapes
  • burns

Warnings

For external use only

Do not use if 

  • in or near the eyes
  • on large areas of the body
    • Ask a doctor before use if you have
    • deep or puncture wounds
    • animal bites
    • serious burns

      • Stop use and ask a doctor if 

      • you need ot use longer than 1 week
      • condition persists or gets worse
      • a rash or other allergic reaction develops

Directions

  • clean the affected area
  • apply a small amount (equal to surface area of tip of finger) on the area 1 to 3 times daily.
  • may be covered with a sterile bandage

Other Information

Store at a controlled room temperature 20°-25°C (68°-77°F)

Inactive Ingredients

Petrolatum 

Questions And Comments ? 1-800-910-6874

Principal Display Panel

Target Up&Up      NDC 11673-892-56

Tripel Anitibiotic Ointment 

Polymxiin B Sulfate 

Bacitracin Zinc

Neomycin Sulfate 

First aid Antibiotic Ointment 

NET WT 1oz(28g)

Total NET WT  2OZ (56g)

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