pilldic.Your medicine dictionary
Text size
← US medicines
US · Over-the-counter medicine

Triple Antibiotic and Pain Relief

Dosage form
OINTMENT
Labeler
Trifecta Pharmaceutical USA LLC
Label updated
2024-12-31
Retrieved
2026-09-07
Active ingredients
BACITRACIN ZINC · NEOMYCIN SULFATE · PRAMOXINE HYDROCHLORIDE
View original label and images on DailyMed ↗
Active Ingredient

Bacitracin zinc 500 Units

Purpose

First Aid Antibiotic

Active Ingredient

Neomycin Sulfate 3.5mg

Purpose

First Aid Antibiotic

Active Ingredient

Polymyxin B Sulfate10,000 Units

Purpose

First Aid Antibiotic

Active Ingredient

Pramoxine HCL 10mg

Purpose

External Analgesic

Uses

First Aid to help prevent infection in minor:

  • Cuts
  • Scrapes
  • 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

Ask a Doctor before Use

Ask Doctor before use if you have:

  • Deep or puncture wounds
  • Animal bites
  • Serious burns
Stop Use and ask a Doctor if:
  • Condition persists or gets worse
  • You need to use longer than 1 week
  • A rash or other allergic reaction develops
Keep out of Reach of Children

If Swallowed, get medical help or contact a Poison Control Center immediately

Directions
  • Clean the affected area and dry thoroughly
  • 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 20° to 25°C (68° to 77°F)
  • See carton or tube crimp for lot number and expiration date
Inactive Ingredient:

Light Mineral Oil, Petrolatum

Questions?

Call 1-800-883-0085

PROUDLY DISTRIBUTED BY: ASSOCIATED WHOLESALE GROCERS, INC.

KANSAS CITY, KANSAS 66106

For product information please visit: bestchoicebrand.com/58315

*Neosporin® + Pain Reliefis a registered trademark of Johnson & Johnson Consumer Inc.

Packaging

[Image in the official label — see DailyMed source]

DailyMed Set ID: 0bf08cf6-be3f-f9aa-e063-6294a90a4393 · Version 2
NDC: 69396-132