QC TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin sulfate , polymyxin b sulfate. ointment 
Chain Drug Marketing Association

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Quality Choice Triple Antibiotic Ointment
First Aid Antibiotic

Drug Facts

Active ingredients (each gram contains)

Bacitracin zinc 400 units
Neomycin sulfate 3.5 mg
Polymyxin B sulfate 5,000 units

Purpose

First Aid Antibiotic Ointment

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

Warnings

For external use only.

Do not use

Stop Use and ask a doctor if

Ask Doctor before use if you have

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

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.

Other information

● To open: unscrew cap, pull tab to remove foil seal

● store at 20° to 25°C ( 68° to 77°F)

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

Inactive ingredientMineral Oil, Petrolatum

Distributed by CDMA., Inc. ©
43157 W 9 Mile Rd.

Novi, MI. 48375

www.qualitychoice.com

Questions: 800-935-2362

Other Information:

This product is not manufactured or distributed by

Johnson & Johnson Corporation, owner of the registered trademark Neosporin®

Packaging

99196 QC TRIPLE ANTIBIOTIC OINTMENT 0.5OZ REV05 030624 CDER

99258 QC TRIPLE ANTIBIOTIC OINTMENT 1OZ REV04 030624 CDER

QC TRIPLE ANTIBIOTIC 
bacitracin zinc, neomycin sulfate , polymyxin b sulfate. ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-050
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
MINERAL OIL (UNII: T5L8T28FGP)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83324-050-011 in 1 BOX05/24/2024
128.3 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:83324-050-051 in 1 BOX03/26/2024
214.2 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00403/15/2024
Labeler - Chain Drug Marketing Association (011920774)
Registrant - Trifecta Pharmaceuticals USA (079424163)

Revised: 6/2024
Document Id: 1a14f49a-8fbc-4b14-e063-6394a90a817b
Set id: 1a1501a4-75b0-5900-e063-6394a90ad77a
Version: 1
Effective Time: 20240604
 
Chain Drug Marketing Association