NEOSPORIN FIRST AID ANTISEPTIC FOAMING FOR KIDS- benzalkonium chloride liquid 
Johnson & Johnson Consumer Inc.

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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NEOSPORIN ® FIRST AID ANTISEPTIC FOAMING LIQUID FOR KIDS ®

Drug Facts

Active ingredient

Benzalkonium Cl 0.13%

Purpose

First aid antiseptic

Uses

first aid to help prevent infection in minor:

  • cuts
  • scrapes
  • burns

Warnings

For external use only

Do not use

  • in the eyes
  • over large areas of the body
  • longer than 1 week

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if the condition persists or gets worse

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 on the area 1 to 3 times daily
    • may be covered with a sterile bandage
    • if bandaged, let dry first
  • children under 2 years of age:
    consult a doctor

Other information

  • store at 20° to 25°C (68° to 77°F)
  • protect from freezing

Inactive ingredients

aloe barbadensis leaf juice, citric acid, disodium EDTA, poloxamer 188, sodium chloride, sodium hydroxide, water

Questions?

call toll-free 800-223-0182 or 215-273-8755 (collect)

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 68 mL Bottle Label

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FROM THE
#1 DOCTOR
RECOMMENDED
BRAND

NEOSPORIN ®
BENZALKONIUM CHLORIDE
FIRST AID ANTISEPTIC
FOAMING LIQUID

FOR KIDS
Ages 2 and up

No Sting

Kills Germs to
Help Prevent Infection

2.3 fl oz (68 mL)

PRINCIPAL DISPLAY PANEL - 68 mL Bottle Label
NEOSPORIN FIRST AID ANTISEPTIC FOAMING FOR KIDS 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0220
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
POLOXAMER 188 (UNII: LQA7B6G8JG)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0220-268 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/01/200910/18/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/01/200910/18/2023
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: ee484505-3bb3-2989-e053-2995a90aea2b
Set id: 5018028a-00b6-46e5-ac12-103b7c5213a6
Version: 4
Effective Time: 20230112
 
Johnson & Johnson Consumer Inc.