Triple Antibiotic Cream
FDA Label NDC 82942-1002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by J&a Digital Inc. for the product Triple Antibiotic (NDC 82942-1002). 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 (in each gram), purpose, uses, warnings, do not use, ask a doctor, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredients (In Each Gram)

Bacitracin zinc (bacitracin 400 units)

Neomycin sulfate (neomycin 3.5 mg)

Polymyxin B sulfate

(polymyxin B 5,000 units)

Purpose

first aid

antibiotic

Uses

first aid to help prevent infection in minor cuts, scrapes, and burns

Warnings

For external use only

Do Not Use

  • in eyes 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 puntucre wounds
  • animal bites
  • serious burns

Stop Use And Ask A Doctor If

  • the condition persists or gets worse
  • a rash or other allergic reaction develops.

Keep Out Of 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 the tip of a finger) on the area 1 to 3 times daily
  • may be covered with a sterile bandage.

Other Information

store at room temperature

Inactive Ingredients

Mineral oil,  petrolatum, purified water

* Please review the disclaimer below.