TRIPLE ANTIBIOTIC AND PAIN RELIEF- bacitracin,neomycin,polymyxinb,pramoxine ointment 
Trifecta Pharmaceutical USA LLC

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Best Choice Triple Antibiotic Ointment + Pain Relief

DRUG FACTS

Active Ingredient

Bacitracin zinc 500 Units

Purpose

First Aid Antibiotic

Active Ingredient

Neomycin Sulfate 3.5mg

Purpose

First Aid Antibiotic

Active Ingredient

Polymyxin B Sulfate10,000 Units

Purpose

First Aid Antibiotic

Active Ingredient

Pramoxine HCL 10mg

Purpose

External Analgesic

Uses

First Aid to help prevent infection in minor:

Warnings

For external use only. Do not use:

Ask a Doctor before Use

Ask Doctor before use if you have:

Stop Use and ask a Doctor if:

Keep out of Reach of Children

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

Directions

Other Information

Inactive Ingredient:

Light Mineral Oil, Petrolatum

Questions?

Call 1-800-883-0085

PROUDLY DISTRIBUTED BY: ASSOCIATED WHOLESALE GROCERS, INC.

KANSAS CITY, KANSAS 66106

For product information please visit: bestchoicebrand.com/58315

*Neosporin® + Pain Reliefis a registered trademark of Johnson & Johnson Consumer Inc.

Packaging

Best Choice Triple Antibiotic Pain Relief Ointment 1oz 050923 CDER

TRIPLE ANTIBIOTIC AND PAIN RELIEF 
bacitracin,neomycin,polymyxinb,pramoxine ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69396-132
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC500 [USP'U]  in 100 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE3.5 mg  in 100 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 100 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 [USP'U]  in 100 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69396-132-011 in 1 BOX12/07/2023
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 DrugM00412/07/2023
Labeler - Trifecta Pharmaceutical USA LLC (079424163)

Revised: 12/2023
Document Id: 0bf08cf6-be40-f9aa-e063-6294a90a4393
Set id: 0bf08cf6-be3f-f9aa-e063-6294a90a4393
Version: 1
Effective Time: 20231207
 
Trifecta Pharmaceutical USA LLC