Medicine guide

Sunmark Triple Antibiotic Plus Pain Relief

500 [iU]/g + 3.5 mg/g + 10000 [iU]/g + 10 mg/g · Ointment

  • Available without prescription
  • Aminoglycoside Antibacterial
Made by
A-S Medication Solutions

Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.

At a glance

Quoted from the official label · 2024-10-22

What it is

Active ingredients (in each gram) Purposes Bacitracin 500 units First aid antibiotic Neomycin 3.5 mg First aid antibiotic Polymyxin B 10,000 units First aid antibiotic Pramoxine HCl 10 mg Topical pain reliever

Used for
  • Cuts scrapes burns
Do not take it if

If you are allergic to any of the ingredients

All warnings ↓
Good to know
  • Sold without a prescription
  • FDA enforcement reports list no ongoing recall, and none from the last two years, for this product code · checked 2026-10-02
1other products contain Polymyxin B Sulfate, Bacitracin Zinc, Neomycin Sulfate, and Pramoxine Hydrochloride — compare makers, forms and strengths

Every line above is selected, not written, from the official label. Nothing is reworded. DailyMed

What it is for

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

  • cuts scrapes burns

From the official label · 2024-10-22 · DailyMed

Do not take it if

if you are allergic to any of the ingredients

Quoted from the official label, section “OTC — Do Not Use”.

How to take it

These directions are for this exact strength and form. Another one is different.

  • unscrew cap and pull tab to remove foil seal
  • adults and
  • children 2 years of age and 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

Quoted from the official label, section “Dosage & Administration”.

Ask a doctor first if

deep or puncture wounds animal bites serious burns

Quoted from the official label, section “OTC — Ask Doctor”.

Stop and get help if

you need to use for more 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

Quoted from the official label, section “OTC — Stop Use”.

Other warnings

  • For external use only
  • Do not use
  • Ask a doctor before use
  • if you have deep or puncture wounds animal bites serious burns
  • When using this product
  • do not use in the eyes do not apply over large areas of the body
  • Stop use and
  • ask a doctor
  • if you need to use for more 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.
  • do not use in the eyes do not apply over large areas of the body

Quoted from the official label, section “Warnings”.

Keep away from children

If swallowed get medical help or contact a Poison Control Center right away

Quoted from the official label, section “OTC — Keep Out of Reach of Children”.

What it looks like and how it is packed

Product: 50090-6172 NDC: 50090-6172-0 28.4 g in a TUBE / 36 in a CASE

Quoted from the official label, section “How Supplied”.

How to store it

store at controlled room temperature 15°-30°C (59°-86°F) see carton or tube crimp for lot number and expiration date

Quoted from the official label, section “Storage and Handling”.

What kind of medicine it is

Active ingredients (in each gram) Purposes Bacitracin 500 units First aid antibiotic Neomycin 3.5 mg First aid antibiotic Polymyxin B 10,000 units First aid antibiotic Pramoxine HCl 10 mg Topical pain reliever

Quoted from the official label, section “OTC — Purpose”.

Other ingredients

Relevant if you react to a dye, a preservative, lactose or gluten.

white petrolatum

Quoted from the official label, section “Inactive Ingredients”.

Ingredients people check for

Lactose, gluten, dyes, sugars and other ingredients that matter with an allergy, intolerance or diet — as this product’s FDA label lists them.

This label’s list of inactive ingredients names none of: lactose, wheat or gluten, colour dyes, sugars, sugar alcohols, alcohol (ethanol), aspartame (phenylalanine), gelatin, peanut oil, soy, parabens, sulfites, titanium dioxide.

Quoted from the FDA label. A label that does not name an ingredient is not a guarantee that the product is free of it, and formulations change. With an allergy, check the pack and ask a pharmacist.

Every version of this medicine (18)

The same active substance, strength and kind of form, from every company that sells it — with what each label lists.

Showing 18 of 18

Details

Made byA-S Medication Solutions
Active substancePolymyxin B Sulfate, Bacitracin Zinc, Neomycin Sulfate, and Pramoxine Hydrochloride
Used inAntibiotics, antivirals and antifungals taken into the body
Strength500 [iU]/g + 3.5 mg/g + 10000 [iU]/g + 10 mg/g
FormOintment
RouteTopical
Packs36 TUBE in 1 CASE / 28.4 g in 1 TUBE
NDC50090-6172

Source: NDC Directory · 2026-09-13 · not reviewed by a clinician

Source: US Food and Drug Administration, NDC Directory. Reuse terms: US government work (FDA).

Other strengths and forms

2 products are sold under this name. Grouped by form; a number on a strength means several companies make it.

  • Ointment2 products
    • 500 [iU]/g + 3.5 mg/g + 10000 [iU]/g + 10 mg/g2

      500 [iU]/g + 3.5 mg/g + 10000 [iU]/g + 10 mg/g · 2 companies

Same active substance

These contain the same substance. That does not mean one can replace another — ask a pharmacist.