Quick answers
- What is Bacitracin zinc, lidocaine, neomycin sulfate and polymyxin b sulfate used for?
- The Drug Facts label of Drs. pharmacy triple antibiotic plus lidocaine (Ol Pharma Tech, LLC) lists these uses: First aid to help prevent infection and temporary relief of pain in minor: cuts scrapes burns.
- Do I need a prescription for Bacitracin zinc, lidocaine, neomycin sulfate and polymyxin b sulfate?
- 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 zinc, lidocaine, neomycin sulfate and polymyxin b sulfate 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.
Drs. pharmacy triple antibiotic plus lidocaine · Ol Pharma Tech, LLC
Bacitracin zinc 500 [USP'U]/g · Lidocaine 4% · Neomycin sulfate 0.35% · Polymyxin b sulfate 10000 [USP'U]/g, ointment (topical)
Active ingredient
Bacitracin Zinc 400 units Neomycin Sulfate 3.5mg Polymyxin B Sulfate 5,000 units Lidocaine 40 mg
Purpose
First aid antibiotic
Uses
First aid to help prevent infection and temporary relief of pain in minor: cuts scrapes burns
Warnings
For external use only
Do not use
do not use in the eyes do not apply over large areas of the body if you are allergic to any of the ingredients longer than one week unless directed by your doctor in large quantities, particularly over raw surfaces or blistered areas Ask a doctor
Ask a doctor before use if
you have serious burns deep or puncture wounds animal bites Stop use and ask a doctor
Stop use and ask a doctor if
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 the reach of children If swallowed, get medical help or contact a Poison Control Center right away
Directions
adults and children 2 years of age and older: clean the affected area apply a small amount of this product (an amount equal tot the surface area of the tip of a finer) 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 room temperature( 68 to 77 F)
Inactive ingredients
Petrolatum
Questions?
Call: 248 325 4231
— FDA label of Drs. pharmacy triple antibiotic plus lidocaine, Ol Pharma Tech, LLC, effective January 30, 2026. See the official label on DailyMed →
Neosporin Plus Lidocaine · Kenvue Brands LLC
Bacitracin zinc 500 [iU]/g · Lidocaine 4% · Neomycin sulfate 0.35% · Polymyxin b sulfate 10000 [iU]/g, ointment (topical)
Active ingredient (in each gram)
Purpose Bacitracin Zinc (500 units) First aid antibiotic Lidocaine (40 mg) External analgesic Neomycin Sulfate (3.5 mg) First aid antibiotic Polymyxin B sulfate (10,000 units) First aid antibiotic
Purpose
Active ingredients (in each gram) Purpose Bacitracin Zinc (500 units) First aid antibiotic Lidocaine (40 mg) External analgesic Neomycin Sulfate (3.5 mg) First aid antibiotic Polymyxin B sulfate (10,000 units) First aid antibiotic
Uses
first aid to help prevent infection and for the 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 in large quantities, particularly over raw surfaces or blistered areas
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 Centre right away.
Directions
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
Inactive ingredients
Petrolatum
Questions?
Call 800-223-0182 or 215-273-8755 (collect)
— FDA label of Neosporin Plus Lidocaine, Kenvue Brands LLC, effective November 24, 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 zinc 500 [USP'U]/g · Lidocaine 4% · Neomycin sulfate 0.35% · Polymyxin b sulfate 10000 [USP'U]/g · ointment (topical) · 2 products
Bacitracin zinc 500 [iU]/g · Lidocaine 4% · Neomycin sulfate 0.35% · Polymyxin b sulfate 10000 [iU]/g · ointment (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Neosporin Plus Lidocaine | Kenvue Brands LLC | DailyMed |
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.
- Kenvue Brands LLC1 product
- Ol Pharma Tech, LLC1 product
- Trifecta Pharmaceuticals USA LLC1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
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.