TRIPLE ANTIBIOTIC PLUS PAIN RELIEF- bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment 
Chain Drug Marketing Association Inc.

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Quality Choice Triple Antibiotic Ointment Plus Pain Relief

Active ingredients (each gram contains)

Bacitracin zinc 400 units



Neomycin sulfate 3.5 mg



Polymyxin B sulfate 5,000 units

Purpose

First aid antibiotic

Active Ingredient

Pramoxine HCL

Purpose

External Analgesic

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

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

WarningsFor external use only.

Do not use● in the eyes ● over large areas of the body

● if you are allergic to any of the ingredients.

Ask a doctor before use if you have

● deep or puncture wounds ● animal bites ● serious burns.

Stop use and ask a doctor ifcondition persists or gets worse

● you need to use longer than 1 week

● a rash or other allergic reaction develops

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.

Inactive ingredient Light Mineral Oil,Petrolatum

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.

Other Information

Distributed by CDMA., Inc.

Novi, MI 48375

www.qualitychoice.com

questions: 800-935-2362

Packaging

94594 QC TRIPLE ANTIBIOTIC PAIN RELIEF OINTMENT 1OZ REV05 020224 CDER

TRIPLE ANTIBIOTIC PLUS PAIN RELIEF 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-036
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [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 B10000 [USP'U]  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83324-036-011 in 1 BOX02/28/2024
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 DrugM00402/28/2024
Labeler - Chain Drug Marketing Association Inc. (011920774)
Registrant - Trifecta Pharmaceuticals USA LLC. (079424163)

Revised: 2/2024
Document Id: 12779daa-01fe-aa1b-e063-6394a90a4d30
Set id: 1277942d-753f-ab69-e063-6394a90a496a
Version: 1
Effective Time: 20240228
 
Chain Drug Marketing Association Inc.