ANTIBIOTIC Maximum Strength
ANTIBIOTIC Maximum Strength is an FDA drug label for the active ingredient BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE manufactured by Walgreens Co. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260512.
- Generic name
- BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE
- Manufacturer
- Walgreens Co.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 0363-1331
- Application
- M004
- Label effective
- 20260512
About this product
ANTIBIOTIC Maximum Strength is an FDA-registered drug product whose active ingredient is BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE. It is labelled by Walgreens Co. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 0363-1331, application M004, label effective 20260512. It is one of 26 FDA drug label records sharing the active ingredient BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE are most often described in connection with: first aid, help prevent, infection minor, cuts scrapes. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
USE(S) First aid to help prevent infection in minor cuts scrapes burns
Dosage & Administration
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
Warnings
WARNINGS For external use only.
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View labelHow products containing BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE compare
FDA lists 26 drug label records with BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Orazen Inc | 5 |
| — | — | Nantong Health & Beyond Hygienic Products Inc. | 3 |
| — | — | ORAZEN INC | 2 |
| — | — | Vive Health LLC | 2 |
| — | — | Walgreens Co. | 2 |
Frequently asked questions
What is ANTIBIOTIC Maximum Strength used for?
USE(S) First aid to help prevent infection in minor cuts scrapes burns
Who makes ANTIBIOTIC Maximum Strength?
Walgreens Co. is the labeler of record for ANTIBIOTIC Maximum Strength. 26 FDA label records share the active ingredient BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does ANTIBIOTIC Maximum Strength come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is ANTIBIOTIC Maximum Strength prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Are there other products containing BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE?
Yes. 26 FDA drug label records list BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has ANTIBIOTIC Maximum Strength been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.