TRIPLE ANTIBIOTIC AND PAIN RELIEF- triple antibiotic ointment 
Target Corporation

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Target Up &Up Maximum Strength Triple Antibiotic+Pain Relief 

Drug Facts 

Active ingredients (in each gram)

Bacitracin 500

Neomycin 3.5 mg

Polymyxin B 10,000 units

Pramoxine HCL 10 mg

Purpose

First aid antibiotic

First aid antibiotic

First aid antibiotic

Pain Relief

Uses

helps prevent infection in and temporarily relieves pain due to minor:

Warnings
For external use only 

Do not use

Ask a doctor before use if you have

Stop use and ask a doctor if 

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

Directions

Other information 

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

Inactive ingredient

Petrolatum 

Questions or comments? 1-800-910-6874

Principal Display panel 

Target Up & Up    NDC 11673-746-28

Maximum Strength Pain Relieving 

First aid Antibiotic Ointment 

Polymixin B Sulfate/Bacitracin Zinc/Neomycin Sulfate/ Pramoxine HCl

NET WT 1.0 OZ (28g)

291001 Tube

591001 Carton

TRIPLE ANTIBIOTIC AND PAIN RELIEF 
triple antibiotic ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-746
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 [USP'U]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-746-281 in 1 CARTON01/31/2024
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00401/31/2024
Labeler - Target Corporation (006961700)

Revised: 1/2024
Document Id: f358223c-786b-4113-9a59-f5b9dbb9b37d
Set id: 8fda7b8a-72f3-4b92-a229-ac5be0e3b3eb
Version: 2
Effective Time: 20240117
 
Target Corporation