MULTI ACTION- bacitracinzinc,neomycinsulfate,polymyxinbsulfate,pramoxinehcl ointment

Multi Action by

Drug Labeling and Warnings

Multi Action 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 Sulfate 10,000 Units

Purpose

First Aid Antibiotic

Active Ingredient

Pramoxine HCL 10mg

Purpose

External Analgesic

Uses

First Aid to help prevent infection in and for temporary relief of pain or discomfort in minor cuts, scrapes and burns.

Warnings

For external use only. Do not use:

• If you are allergic to any of the ingredients
• in the eyes
• on large areas of the body

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:

• You need to use longer than 1 week
• Condition persists or gets worse
• Symptoms persists for more than 1 week or clear up and occur again within a few days
• A rash or other allergic reaction develops

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:

• Clean the affected area
• 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

Children under 2 years: ask a doctor

Other Information

• Store at 20° to 25°C (68° to 77°F)

Inactive Ingredient:

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

Questions?

Call 1-888-296-9067 Weekdays 9AM - 5PM EST

Other Information

Distributed By

Trifecta Pharmaceuticals USA®

101 NE Third Avenue, Suite 1500

Ft. Lauderdale, FL. 33301 USA

www.trifecta-pharma.com

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

Packaging

INGREDIENTS AND APPEARANCE

MULTI ACTION 
bacitracinzinc,neomycinsulfate,polymyxinbsulfate,pramoxinehcl ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69396-072
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B	10000 [USP'U]  in 1 g
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN ZINC	500 [USP'U]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN SULFATE	3.5 mg  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM PYRUVATE (UNII: POD38AIF08)
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
OLIVE OIL (UNII: 6UYK2W1W1E)
LEVANT COTTONSEED OIL (UNII: N5CFT140R8)
COCOA BUTTER (UNII: 512OYT1CRR)
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69396-072-01	1 in 1 BOX	01/22/2021
1		28.4 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	01/22/2021

Labeler - Trifecta Pharmaceutical USA LLC (079424163)