Band-Aid Brand Hurt-Free Antiseptic Pain Relieving

Manufacturer
Johnson & Johnson Consumer Inc.
Effective date
2023-01-24
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:39:16

Label at a glance#

ProductBand-Aid Brand Hurt-Free Antiseptic Pain Relieving
Active ingredientBENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE
Label structure10 sections

Indications and uses

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

Dosage and administration

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

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredientsPurpose
Benzalkonium Cl 0.13%First aid antiseptic
Lidocaine HCl 2% w/wTopical analgesic

Uses

INDICATIONS & USAGE SECTION

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

  • cuts
  • scrapes
  • burns

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • 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

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

STORAGE AND HANDLING SECTION

  • store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf juice, disodium EDTA, poloxamer 188, sodium chloride, sodium citrate, water

Questions?

OTC - QUESTIONS SECTION

call toll-free 866-565-2873 or 215-273-8755 (collect)

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 177 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BAND-AID ®
BRAND OF FIRST AID PRODUCTS
Johnson & Johnson

HURT-FREE ®
FIRST AID ANTISEPTIC
PAIN RELIEVING LIQUID

For Minor Cuts,
Scrapes, & Burns
Antiseptic to Kill Germs
Helps Prevent Infection

6 FL OZ (177 mL)

Principal Display Panel - 177 mL Bottle Label
Principal Display Panel - 177 mL Bottle Label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69968-022169968-0221-6

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f306e2d4-77d5-ff8f-e053-2a95a90ad15b6c2b9131-050e-4fc3-96e4-57665de2e4132023-01-24WarningsExact identifier
spl id: f306e2d4-77d5-ff8f-e053-2a95a90ad15b
spl set id: 6c2b9131-050e-4fc3-96e4-57665de2e413

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.