Active Ingredients

Manufacturer
OL PHARMA TECH, LLC | OL PHARMA TECH, LLC Drs PHARMACY
Effective date
2026-07-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-07-17 21:45:30

Label at a glance#

ProductDrs pharmacy triple antibiotic Pain plus itch plus Scar
Active ingredientBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE
Label structure13 sections

Indications and uses

First aid to help prevent infection in minor: cuts scrapes burns

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

  • Bacitracin Zinc 500 units
  • Neomycin Sulfate 3.5mg
  • Polymyxin B Sulfate 10,000 units
  • pramoxine HCL 10mg

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

Ask a doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • serious burns
  • deep or puncture wounds
  • animal bites

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition persists or gets worse
  • rash or other allergic reaction develops

Do not use

OTC - DO NOT USE SECTION

  • 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

keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

OTHER SAFETY INFORMATION

  • store at room temperature

Inactive ingredient

INACTIVE INGREDIENT SECTION

Petrolatum

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TRIPLE ANTIBIOTICTRIPLE ANTIBIOTIC

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
99e684e6-f435-feb8-d2bb-3a546f1cb768Product name220161117
25340b3b-3e4c-4ff8-abf6-3e62ec46bd0cProduct name120160603
2d352c73-a357-4193-a4de-dfdf9a2ac8e4Product name120150819
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8Product name120140508
a7051cba-790b-a699-81f8-dbbbdbd9b5acProduct name120140508
b045ad64-0f28-9a02-2f9b-b34d94fb2278Product name120140508
b6082387-f592-1148-0844-bd068fd213fbProduct name120140508
da108d9e-edc8-17a3-8c28-3251c6a8acccProduct name120140508

FDA-Initiated Inactive NDC Indexing#

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80489-41280489-412-01, 80489-412-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12024-04-15full-release2026-06-01 00:11:08

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
Drs pharmacy triple antibiotic Pain plus itch plus ScarBACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE OINTMENTOL PHARMA TECH, LLC16273878-2f58-0d26-e063-6394a90a47d22026-07-09WarningsExact identifier
ndc (package): 80489-412-01
ndc (package): 80489-412-02
ndc (product): 80489-412
ndc11 (package): 80489041202
ndc11 (package): 80489041201
spl id: 563671a0-6672-ab59-e063-6294a90a3c4f
spl set id: 16273878-2f58-0d26-e063-6394a90a47d2

Reported adverse events (FAERS/openFDA)#

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