Publix Triple Antibiotic Ointment
FDA Label NDC 56062-830

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Publix Super Markets, Inc. for the product Publix Triple Antibiotic (NDC 56062-830). 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 ingredient, purpose, uses, warnings, do not use, consult a doctor before use if you have, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Bacitracin 400 units

Neomycin 3.5 mg/g

Polymyxin B 5000 units

Purpose

Bacitracin 400 units..........First aid antibiotic 

Neomycin 3.5 mg/g..........First aid antibiotic 

Polymyxin B 5000 units....First aid antibiotic

Uses

First aid to help prevent infection in minor;

  • cuts 
  • scrapes
  • burns

Warnings

For external use only 

Allergy alert

  • do not use if you are allergic to any of the ingredients

Do Not Use

  • in or near eyes
  • on large area of the body

Consult A Doctor Before Use If You Have

  • deep puncture wounds
  • animal bites
  • serious burns

When Using This Product

do not use longer than 1 week

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 Ingredient

Petrolatum 

Principal Display Panel

Publix Triple Antibiotic Ointment         NDC 56062-830-28

Bacitracin Zinc/ Neomycin Sulfate/ Polymyxin B Sulfate

NET WT 1.0 OZ (28g)

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