FAMILY WELLNESS FIRST AID ANTIBIOTIC- family wellness bacitracin zinc, polymyxin b sulfate ointment 
Trifecta Pharmaceuticals 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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Double Antibiotic Ointment

Active Ingredient

Bacitracin 500 Units

Purpose

First Aid Antibiotic

Active Ingredient

Polymyxin B

Purpose

First Aid Antibiotic

Uses

First aid to help prevent infection in minor

Warnings

For External use only.

Do not use

Ask a doctor before use if you have:

Stop use and ask doctor if:

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

Directions:

Other Information

Store between 20° to 25°C (68° to 77°F)

Inactive Ingredients

Mineral Oil, White Petrolatum

Questions or Comments?

Call 1-888-296-9067 Weekdays 9AM to 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 Consumer Products Company, owner of the registered trademark Polysporin®

MADE IN CHINA

FD Double Antibiotic

FAMILY WELLNESS FIRST AID ANTIBIOTIC 
family wellness bacitracin zinc, polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69396-037
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 [USP'U]  in 1 g
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [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:69396-037-051 in 1 BOX08/30/2019
115 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:69396-037-041 in 1 BOX01/10/2020
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 finalpart333B08/29/2019
Labeler - Trifecta Pharmaceuticals USA, LLC (079424163)

Revised: 1/2023
Document Id: f276d390-8f33-8921-e053-2a95a90a0f2d
Set id: 9157681a-3ed1-096e-e053-2a95a90a05e3
Version: 8
Effective Time: 20230117
 
Trifecta Pharmaceuticals USA, LLC