TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin sulfate , polymyxin b sulfate ointment 
TRIFECTA PHARMACEUTICALS USA LLC

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Best Choice Triple Antibiotic Ointment

Active ingredients (each gram contains)

Bacitracin zinc 400 units

Neomycin sulfate 3.5 mg

Polymyxin B sulfate 5,000 units

Purpose

First aid antibiotic

Keep out of reach of Children

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

Uses

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

Warnings

For external use only.

Directions

● clean the affected area and dry thoroughly.

● 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.

Stop Use and Ask Doctor

Ask Doctor Before Use if you have

Do Not Use

Inactive ingredient light Mineral Oil, Petrolatum

Other information



● store at 20° to 25°C ( 68° to 77°F)

● see carton or tube crimp for lot number and expiration date.

Questions? Call 1-800-883-0085

Distributed By

Proudly Distributed by

Associated Wholesale Grocers Inc.

Kansas City, Kansas 66105

For Product Information please visit: bestchoicebrands.com/58314

Neosporin is a registered trademark of Johnson & Johnson Consumer Inc.

Best Choice Triple Antibiotic Pain Relief Ointment 1oz 050923 CDER

TRIPLE ANTIBIOTIC 
bacitracin zinc, neomycin sulfate , polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69396-131
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN400 [USP'U]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B5000 [USP'U]  in 1 g
Inactive Ingredients
Ingredient NameStrength
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69396-131-011 in 1 BOX12/08/2023
128.3 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00412/08/2023
Labeler - TRIFECTA PHARMACEUTICALS USA LLC (079424163)

Revised: 10/2023
Document Id: 0c017b20-0f95-80e4-e063-6294a90a9550
Set id: 0c017b10-29b6-e30f-e063-6294a90a8a3c
Version: 1
Effective Time: 20231030
 
TRIFECTA PHARMACEUTICALS USA LLC