FDA.reportPublic FDA data

Triple Antibiotic

Manufacturer
Rite Aid Corporation
Effective date
2025-12-29
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
monthly-update
Hydrated at
2026-06-03 17:47:05

Label at a glance#

ProductTriple Antibiotic
Active ingredientBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE
Label structure10 sections

Indications and uses

First aid to help prevent infection and for the temporary relief of pain in minor cuts  scrapes  burns

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredients (in each gram)

OTC - ACTIVE INGREDIENT SECTION

Bacitracin Zinc USP, 500 units

Neomycin 3.5 mg

Polymyxin B sulfate USP, 10,000 units

Pramoxine hydrochloride USP, 10 mg

Purpose

OTC - PURPOSE SECTION

First aid antibiotic

Pain reliever

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent infection and for the temporary relief of pain in minor

  • cuts 
  • scrapes 
  • burns

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • if you are allergic to any of the ingredients
  • in the eyes
  • over large areas of the body

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • you need to use for longer than one week
  • condition persists or gets worse
  • rash or other allergic reaction develops
  • symptoms persist for more than one week, or clear up and occur again with a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

Other information

SPL UNCLASSIFIED SECTION

  • Store at 15º-30ºC (59º-86ºF)
  • Before using any medication, read all label directions. Keep carton, it contains important information.

Inactive ingredient

INACTIVE INGREDIENT SECTION

white petrolatum

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to the active ingredients in Neosporin® + Pain Relief Ointment*

MAXIMUM STRENGTH

TRIPLE ANTIBIOTIC OINTMENT + PAIN RELIEF

BACITRACIN ZINC 

NEOMYCIN SULFATE

POLYMYXIN B SULFATE

PRAMOXINE HCl

FIRST AID ANTIBIOTIC /

PAIN-RELIEVING OINTMENT

FOR EXTERNAL USE ONLY

HELP PREVENTINFECTION AND

TEMPORARILY RELIEVES PAIN OF MINOR CUTS, SCRAPES, AND BURNS

NET WT OZ (g)

*This product is not manufactured or distributed by Johnson & Johnson Consumer, Inc distributor of Neosporin® + Pain Relief Ointment.

DISTRIBUTED BY:

RITE AID, 30 HUNTER LANE,

CAMP HILL, PA 17011

www.riteaid.com

Package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RITE AID Maximum Strength Triple Antibiotic Ointment and Pain relief
RITE AID Maximum Strength Triple Antibiotic Ointment and Pain relief

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130011822212212GTIN-13: 0011822212212
EAN-13: 0011822212212
GTIN-12: 011822212212
UPC-A: 011822212212
GTIN storage (14 digits): 00011822212212		triple-antibiotic-with-pramoxine-ointment-ene-deli-1.jpg

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

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
11822-270011822-2700-5, 11822-2700-1, 11822-2700-2

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
BACITRACIN ZINC89Y4M234ESACTIM
NEOMYCIN SULFATE057Y626693ACTIM
POLYMYXIN B SULFATE19371312D4ACTIM
PRAMOXINE HYDROCHLORIDE88AYB867L5ACTIB
PETROLATUM4T6H12BN9UIACT

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
4da0f3db-db74-4c58-a44b-79221aaf4343c1c9bb83-4f79-4996-8019-9ee382bbf8c72025-12-29WarningsExact identifier
spl id: 4da0f3db-db74-4c58-a44b-79221aaf4343
spl set id: c1c9bb83-4f79-4996-8019-9ee382bbf8c7

Reported adverse events (FAERS/openFDA)#

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