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US · Over-the-counter medicine

Triple Antibiotic plus pain relief

Dosage form
OINTMENT
Labeler
Kroger Company
Label updated
2024-10-06
Retrieved
2026-09-07
Active ingredients
PRAMOXINE HYDROCHLORIDE
View original label and images on DailyMed ↗
Active ingredients (in each gram)

Bacitracin zinc 500 units

Neomycin sulfate equivalent to 3.5 mg of neomycin base

Polymyxin B 10,000 units as polymyxin B sulfate

Pramoxine HCl 10 mg

Purpose

First aid antibiotic

External analgesic

Uses

first aid to help prevent infection and for temporary relief of pain or discomfort in minor:

  • •cuts
  • •scrapes
  • •burns
Warnings

For external use only.

Do not use

  • •if you are allergic to any of the ingredients
  • •in the eyes
  • •over 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 to use longer than 1 week
  • •condition persists or gets worse
  • •symptoms persist for more than 1 week, or clear up and occur again within a few days
  • •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. (1-800-222-1222)

Directions
  • •adults and children 2 years of age or older:
  • •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
  • •children under 2 years of age: ask a doctor
Other information
  • •store at 20-25°C (68-77°F)
Inactive ingredient

white petrolatum

Questions or comments?

1-800-632-6900

Principal Display Panel

COMPARE TO active ingredients of NEOSPORIN® + PAIN RELIEF See back panel

Maximum Strength

Triple Antibiotic + Pain Relieving Ointment

First Aid Antibiotic/Pain Relieving Ointment

Bacitracin Zinc

Neomycin Sulfate

Polymyxin B Sulfate

Pramoxine HCl

NET WT 1 OZ (28g)

[Image in the official label — see DailyMed source]

DailyMed Set ID: e31c8d92-bf9f-4b7f-8f81-54199745cd20 · Version 3
NDC: 30142-679