BAND AID ANTISEPTIC CLEANSING LIQUID- benzalkonium chloride and lidocaine hydrochloride 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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Band Aid Antiseptic Cleansing Liquid

Drug Facts

Benzalkonium Cl (0.13%)

Lidocaine HCl (2%)

Benzalkonium Cl -
First aid antiseptic


Lidocaine HCl - Topical analgesic

Uses

first aid to help prevent infection and temporarily relieve pain or discomfort in minor:

Warnings

For external use only

Do not use

  • in the eyes
  • over large areas of the body
  • in large quantities, particularly over raw surfaces or blistered areas.

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

  • condition or symptoms get worse or last more than 1 week
  • symptoms clear up and occur again within a few days

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

Water, Poloxamer 188, Sodium Chloride, Disodium EDTA, Sodium Citrate, Aloe Barbadensis Leaf Juice

Questions?

Call 800-526-3967 or 215-273-8755 (collect).

Distributed by:

JOHNSON & JOHNSON CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 177 mL Bottle Label

BAND-AID ®

BRAND OF FIRST AID PRODUCTS

Johnson & Johnson

ANTISEPTIC CLEANSING

LIQUID

FIST AID ANTISEPTIC PAIN RELIEVING LIQUID

Kills 99.99% of germs* to prevent infections

No sting

Relieves pain with lidocaine

For minor cuts,
scrapes, & burns


6 FL OZ (177 mL)

PRINCIPAL DISPLAY PANEL - 177 mL Bottle Label

BAND AID ANTISEPTIC CLEANSING LIQUID 
benzalkonium chloride and lidocaine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0730
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
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
POLOXAMER 188 (UNII: LQA7B6G8JG)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0730-6177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/03/2022
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: ef3852ba-33ef-2adb-e053-2995a90ae32e
Set id: d2a6e0d2-5b9b-11c0-e053-2a95a90a4df0
Version: 4
Effective Time: 20230109
 
Johnson & Johnson Consumer Inc.