Sheffield Triple Antibiotic Plus Pain Relief
Generic: Bacitracin Zinc, Polymyxin B Sulfate, Neomycin Sulfate, Pramoxine Hydrochloride
✓ FDA-verified
View full FDA label ↗Sheffield Triple Antibiotic Plus Pain Relief is a topical medication that helps prevent infections and temporarily relieve pain from cuts, scrapes, and burns. It works by fighting bacteria and reducing discomfort in the affected area. To use it, clean the area and apply a small amount, about the size of your fingertip, one to three times a day, and you can cover it with a sterile bandage if needed. It's important to note that you should not use this medication for more than one week, and if your condition doesn't improve or gets worse, you should see a doctor. Additionally, do not use it if you are allergic to any of its ingredients.
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Uses
- cuts. scrapes. burns.
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Dosage
Clean the affected area before use.
Apply a small amount equal to the tip of your finger.
Use 1 to 3 times daily.
May be covered with a sterile bandage.
Always follow your doctor's specific instructions for your dose.
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Side effects
Common
Condition may persist or worsenSymptoms lasting more than 7 daysSymptoms clearing up and returning within a few days
Serious
Possible rash or allergic reaction
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Warnings
⚠ Important warnings
- For external use only.
- Do not use if allergic to any ingredients.
- Avoid using in or near the eyes.
- Do not use on large areas of the body.
- Consult a doctor for deep or puncture wounds, animal bites, or serious burns.
- Do not use longer than 1 week.
- Keep out of reach of children.
- If swallowed, seek medical help immediately.
Ask about this product
Answers pulled from the FDA label only.
Medical Disclaimer: This content is provided for informational and educational purposes only and is not intended as medical advice. Always consult a qualified healthcare provider before taking any medication.
Data Source: Publicly available drug labeling information from the U.S. Food and Drug Administration (FDA).
Data Source: Publicly available drug labeling information from the U.S. Food and Drug Administration (FDA).
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