POLVO DE SULFA FIRST AID ANTIBIOTIC

Manufacturer
Coastal Contract Packaging, Inc.
Effective date
2025-06-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:36:51

Label at a glance#

ProductPOLVO DE SULFA FIRST AID ANTIBIOTIC
Active ingredientBACITRACIN ZINC, POLYMYXIN B SULFATE
Label structure8 sections

Indications and uses

First aid to help prevent infection in minor cuts scrapes burns

Dosage and administration

Adults and children 2 years of age and older: clean the affected area apply a light dusting of the powder on the area 1 to 3 times daily may be covered with a sterile bandage Children under 2 years of age: consult a doctor

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

BACITRACIN ZINC 500 UNITS

POLYMYXIN B SULFATE 10,000 UNITS

Purpose:

OTC - PURPOSE SECTION

First aid antibiotic

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent infection in minor

  • cuts
  • scrapes
  • burns

Warnings

WARNINGS SECTION

  • For external use only

Do not use

  • in the eyes
  • if you are allergic to any of the ingredients
  • over large areas of the body
  • longer than 1 week unless directed by doctor

Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns

Stop use and ask a doctor if

  • the conditions persists or gets worse
  • a rash or other allergic reaction develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childern.If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older:

  • clean the affected area
  • apply a light dusting of the powder on the area 1 to 3 times daily
  • may be covered with a sterile bandage

Children under 2 years of age: consult a doctor

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Lactose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

frontfront

backback

Products#

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DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42523-11542523-115-75

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
37b88f6e-726a-eb56-e063-6294a90a072d37b88f6e-7269-eb56-e063-6294a90a072d2025-06-16WarningsExact identifier
spl id: 37b88f6e-726a-eb56-e063-6294a90a072d
spl set id: 37b88f6e-7269-eb56-e063-6294a90a072d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.