NEOSPORIN FIRST AID ANTISEPTIC FOAMING FOR KIDS- benzalkonium chloride liquid

Neosporin First AID Antiseptic Foaming for Kids by

Drug Labeling and Warnings

Neosporin First AID Antiseptic Foaming for Kids by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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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)

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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)

INGREDIENTS AND APPEARANCE

NEOSPORIN FIRST AID ANTISEPTIC FOAMING FOR KIDS 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0220
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0220-2	68 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	06/01/2009

Labeler - Johnson & Johnson Consumer Inc. (002347102)