TRIPLE ANTIBIOTIC AND PAIN RELIEF- bacitracin,neomycin,polymyxinb,pramoxine ointment

Triple Antibiotic and Pain Relief by

Drug Labeling and Warnings

Triple Antibiotic and Pain Relief by is a Otc medication manufactured, distributed, or labeled by Trifecta Pharmaceutical USA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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:

• Cuts
• Scrapes
• Burns

Warnings

For external use only. Do not use:

• In eyes
• Over large areas of the body
• If you are allergic to any of the ingredients

Ask a Doctor before Use

Ask Doctor before use if you have:

• Deep or puncture wounds
• Animal bites
• Serious burns

Stop Use and ask a Doctor if:

• Condition persists or gets worse
• You need to use longer than 1 week
• A rash or other allergic reaction develops

Keep out of Reach of Children

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

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

Other Information

• Store at 20° to 25°C (68° to 77°F)
• See carton or tube crimp for lot number and expiration date

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

INGREDIENTS AND APPEARANCE

TRIPLE ANTIBIOTIC AND PAIN RELIEF 
bacitracin,neomycin,polymyxinb,pramoxine ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69396-132
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN ZINC	500 [USP'U]  in 100 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN SULFATE	3.5 mg  in 100 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	10 mg  in 100 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B	10000 [USP'U]  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
LIGHT MINERAL OIL (UNII: N6K5787QVP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69396-132-01	1 in 1 BOX	12/07/2023
1		28.3 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M004	12/07/2023

Labeler - Trifecta Pharmaceutical USA LLC (079424163)