NEOSPORIN PLUS PAIN RELIEF  NEO TO GO - bacitracin zinc, neomycin sulfate, polymyxin b sulfate and pramoxine hydrochloride ointment 
Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

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NEOSPORIN PLUS PAIN RELIEF

Drug Facts

Active ingredients (in each gram)	Purpose
Bacitracin 500 units	First aid antibiotic
Neomycin 3.5 mg	First aid antibiotic
Polymyxin B 10,000 units	First aid antibiotic
Pramoxine HCl 10 mg	External analgesic

Uses

first aid to help prevent infection and for temporary relief of pain or discomfort in minor:

• cuts
• scrapes
• burns

Warnings

For external use only.

Do not use

• if you are allergic to any of the ingredients
• in the eyes
• over large areas of the body

Ask a 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 persist for more than 1 week, or clear up and occur again within a few days
• 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 of age 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 of age: ask a doctor

Other information

• store at 20° to 25°C (68° to 77° F)

Inactive ingredient

white petrolatum

Questions?

call 1-800-223-0182

PRINCIPAL DISPLAY PANEL - 3.7 g Carton

NEOSPORIN®+PAIN RELIEF

NEO TO GO!®

Bacitracin Zinc-Neomycin Sulfate-Polymyxin B Sulfate-Pramoxine HCl
FIRST AID ANTIBIOTIC/PAIN RELIEVING OINTMENT

NEW
PUMP

SPECIALLY
DESIGNED
EASY, ONE-HANDED USE

RESISTS CRUSHING
Infection Protection, Anytime, Anywhere

NET WT 0.13 oz (3.7 g)

NEOSPORIN PLUS PAIN RELIEF   NEO TO GO bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride   ointment

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 58232-9612 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Bacitracin Zinc (Bacitracin Zinc) Bacitracin Zinc 500 [iU]  in 1 g Neomycin Sulfate (Neomycin) Neomycin Sulfate 3.5 mg  in 1 g Polymyxin B Sulfate (Polymyxin B) Polymyxin B Sulfate 10000 [iU]  in 1 g Pramoxine Hydrochloride (Pramoxine) Pramoxine Hydrochloride 10 mg  in 1 g

Inactive Ingredients Ingredient Name Strength Petrolatum

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 58232-9612-1 1 BOTTLE In 1 BLISTER PACK contains a BOTTLE, PUMP 1 3.7 g In 1 BOTTLE, PUMP This package is contained within the BLISTER PACK (58232-9612-1)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333B	02/01/2011

Labeler - Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. (830803164)

Revised: 01/2011Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.