FAMILY WELLNESS PAIN SCAR ITCH- bacitracin zinc, neomycin sulfate, polymyxin b, pramoxine hcl ointment 
Trifecta Pharmaceutical USA LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Triple Antibiotic Pain Scar Itch

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

Pain Reliever

Uses

Helps prevent infection in and temporarily relieves pain due to minor cuts, scrapes and burns.

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:

When using this product

Do not use longer than 1 week

Keep out of Reach of Children

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

Directions

Adults and children 2 years and older:

Children under 2 years: ask a doctor

Other Information

Inactive Ingredient:

Cocoa Butter, Levant Cottonseed Oil, Olive Oil, Petrolatum, Sodium pyruvate, vitamin E

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

69396-054-01 fd pain scar itch SKU 999855 2.11.20

FAMILY WELLNESS PAIN SCAR ITCH 
bacitracin zinc, neomycin sulfate, polymyxin b, pramoxine hcl ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69396-054
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC500 [USP'U]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE3.5 mg  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 [USP'U]  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
COCOA BUTTER (UNII: 512OYT1CRR)  
LEVANT COTTONSEED OIL (UNII: N5CFT140R8)  
SODIUM PYRUVATE (UNII: POD38AIF08)  
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
OLIVE OIL (UNII: 6UYK2W1W1E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69396-054-011 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 finalpart333B08/30/2019
Labeler - Trifecta Pharmaceutical USA LLC (079424163)

Revised: 1/2023
Document Id: f276f813-a268-42ad-e053-2a95a90a70fd
Set id: 9e507ec5-310d-3a21-e053-2a95a90a15a6
Version: 2
Effective Time: 20230117
 
Trifecta Pharmaceutical USA LLC