BAND AID ANTISEPTIC CLEANSING TO GO- benzalkonium chloride, pramoxine hcl spray

Band Aid Antiseptic Cleansing To Go by

Drug Labeling and Warnings

Band Aid Antiseptic Cleansing To Go 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%)

Pramoxine HCl (1%)

Purposes

First aid antiseptic

Topical analgesic

Use

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

Warnings

• For external use only.

Do not use · in the eyes · over large area 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 · 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

adults and children 2 years of age and older:

clean the affected area
spray 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

Protect from freezing

Inactive ingredients

Water, Propylene Glycol, Disodium EDTA

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 7.7mL Vial Blister pack

BAND-AID®

BRAND OF FIRST AID PRODUCTS

Johnson & Johnson

ANTISEPTIC

CLEANSING

TO-GO-SPRAY

FIRST AID ANTIBIOTIC

PAIN RELEIVING SPRAY

Kills 99.99% of germs*

to prevent infection

No sting

Plus pain relief

OVER 140 SPRAYS

FOR EXTERNAL USE ONLY

0.26 FL OZ (7.7mL)

For minor cuts,

scrapes & burns

INGREDIENTS AND APPEARANCE

BAND AID ANTISEPTIC CLEANSING TO GO 
benzalkonium chloride, pramoxine hcl spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0727
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	10 mg  in 1 mL
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0727-1	6 in 1 PACKAGE	01/30/2022
1		1 in 1 BLISTER PACK
1		7.7 mL in 1 VIAL; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/30/2022

Labeler - Kenvue Brands LLC (118772437)