Quick answers
- What is Bacitracin, neomycin, polymyxin b and pramoxine used for?
- The Drug Facts label of Tripleantibioticointmentandpainrelief (Trifecta Pharmaceuticals USA) lists these uses: First Aid to help prevent infection in minor: Cuts Scrapes Burns.
- Do I need a prescription for Bacitracin, neomycin, polymyxin b and pramoxine?
- No. The products on this page are sold without a prescription (over the counter).
- Is a store brand the same as the name brand?
- Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
- Has Bacitracin, neomycin, polymyxin b and pramoxine been recalled?
- No recall linked to these products appears in the FDA enforcement reports we use.
Drug Facts label
Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.
Tripleantibioticointmentandpainrelief · Trifecta Pharmaceuticals USA
Bacitracin 500 [USP'U]/100 g · Neomycin sulfate 3.5 mg/100 g · Polymyxin b sulfate 10000 [USP'U]/100 g · Pramoxine hydrochloride 10 mg/100 g, ointment (topical)
Active ingredient
Bacitracin Zinc 500 Units Active Ingredient Neomycin 3.5mg Active Ingredient Polymyxin B 10,000 Units Active Ingredient Pramoxine HCL 10mg
Purpose
First Aid Antibiotic Purpose First Aid Antibiotic Purpose First Aid Antibiotic 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 wouns 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 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
Inactive ingredients
mineral oil, white Petrolatum
Questions?
Call 1-888-296-9067
— FDA label of Tripleantibioticointmentandpainrelief, Trifecta Pharmaceuticals USA, effective October 22, 2025. See the official label on DailyMed →
This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.
Same medicine, other brands
Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.
Bacitracin 500 [USP'U]/100 g · Neomycin sulfate 3.5 mg/100 g · Polymyxin b sulfate 10000 [USP'U]/100 g · Pramoxine hydrochloride 10 mg/100 g · ointment (topical) · 4 products
Companies that sell this medicine
The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.
- Trifecta Pharmaceuticals USA2 products
- Trifecta Pharmaceutical USA LLC2 products
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Next steps
- Find a pharmacy near youA pharmacist can answer questions about this label
- Latest FDA drug recallsPrescription and over-the-counter, newest first
- All over-the-counter medicinesSearch by ingredient, brand or Spanish name
Sources
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- FDA rule for the Drug Facts label (21 CFR 201.66)
Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.