TRIPLEANTIBIOTICOINTMENTANDPAINRELIEF- family wellness bacitracin,neomycin,polymyxinb,pramoxine ointment 
Trifecta Pharmaceutical USA LLC

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Triple Antibiotic Ointment + Pain Relief

DRUG FACTS

Active Ingredient

Bacitracin 500 Units

Purpose

First Aid Antibiotic

Active Ingredient

Neomycin 3.5mg

Purpose

First Aid Antibiotic

Active Ingredient

Polymyxin B 10,000 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 right away

Directions

Other Information

Inactive Ingredient:

Petrolatum

Questions?

Call 1-888-296-9067

Weekdays 9AM - 4PM EST

DISTRIBUTED BY: MIDWOOD BRANDS, LLC.

500 Volvo Parkway, Chesapeake, VA. 23320

NOT SATISFIED?

Return package and unused product within 30 days to any Family Dollar store for a refund (with receipt) or exchange.

This product is not manufactured or distributed by Johnson & Johnson Corporation, owner of the registered trademark Neosporin® Plus Pain Relief.

Packaging

family wellness triple antibiotic plus pain ointment

TRIPLEANTIBIOTICOINTMENTANDPAINRELIEF 
family wellness bacitracin,neomycin,polymyxinb,pramoxine ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69396-044
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69396-044-011 in 1 BOX09/22/2019
128.4 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00408/30/2019
Labeler - Trifecta Pharmaceutical USA LLC (079424163)

Revised: 12/2024
Document Id: 29b3e33a-544c-40b4-e063-6394a90a1107
Set id: 91575333-5268-5d8f-e053-2a95a90a7a89
Version: 4
Effective Time: 20241220
 
Trifecta Pharmaceutical USA LLC