CURAD MAXIMUM STRENGTH TRIPLE ANTIBIOTIC- bacitracin, neomycin, polymyxin b, pramoxine hydrochloride ointment 
Medline Industries, LP

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031 Curad Maximum Strength Triple Antibiotic

Active ingredients (in each gram)

Bacitracin 500 units

Neomycin 3.5 mg

Polymyxin B 10,000 units

Pramoxin hydrochloride 10 mg

Purposes

First aid antibiotic

First aid antibiotic

First aid antibiotic

Pain reliever

Uses

Warnings

Do not use

  • if allergic to any of the ingredients
  • in or near the eyes
  • on large areas of the body

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

  • you need to use longer than 1 week
  • condition lasts or gets worse
  • symptoms last for more than 7 days, or clear up and come back within a few days
  • a rash or other allergic reaction develops

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Adults and children 2 years and older:

Children under 2 years: ask a doctor

Other information

Store at controlled room temperature 68º-77ºF (20º-25ºC).

Inactive ingredient

petrolatum

Manufacturing Information

Manufactured for:

Medline Industries, LP

Three Lakes Drive Northfield, IL 60093 USA


www.curad.com

1-800-MEDLINE (633-5463)

REF: CUR001232

Package Label

label

CURAD MAXIMUM STRENGTH TRIPLE ANTIBIOTIC 
bacitracin, neomycin, polymyxin b, pramoxine hydrochloride ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-031
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 [USP'U]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE3.5 mg  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 g
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC500 [USP'U]  in 1 g
Inactive Ingredients
Ingredient NameStrength
WHITE PETROLATUM (UNII: B6E5W8RQJ4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53329-031-011 in 1 BOX12/01/2019
128.4 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00412/01/2019
Labeler - Medline Industries, LP (025460908)

Revised: 7/2025
Document Id: 38e2de4d-a347-7416-e063-6294a90a7a94
Set id: 99e9c394-ebf1-7a27-e053-2a95a90ab157
Version: 6
Effective Time: 20250701
 
Medline Industries, LP