AMERICAN RED CROSS ANTISEPTIC CLEANSING- benzalkonium chloride spray

American Red Cross Antiseptic Cleansing by

Drug Labeling and Warnings

American Red Cross Antiseptic Cleansing by is a Otc medication manufactured, distributed, or labeled by MY IMPORTS USA, LLC, KOZMO KIMYA SANAYI VE DIS TICARET LIMITED SIRKETI CORLU SUBESI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Cl 0.13% w/v

Purpose

First aid antiseptic

Uses

First aid to help prevent the risk of bacterial contamination or skin infection associated with minor:  cuts scrapes burns.

Warnings

For external use only.

Do not use

in or near the eyes
over large areas of the body or in large quantities
longer than I week
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 I 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 or excessive heat  store at room temperature. 

Inactive ingredients

Water (Aqua), Propylene Glycol, Lactic acid

Package Labeling:

INGREDIENTS AND APPEARANCE

AMERICAN RED CROSS ANTISEPTIC CLEANSING 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51628-0035
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
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
LACTIC ACID (UNII: 33X04XA5AT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51628-0035-1	177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	11/01/2025

Labeler - MY IMPORTS USA, LLC (195767988)

Registrant - KOZMO KIMYA SANAYI VE DIS TICARET LIMITED SIRKETI CORLU SUBESI (751128462)