AMERICAN RED CROSS FIRST AID- benzalkonium chloride, lidocaine hydrochloride spray

American Red Cross First Aid by

Drug Labeling and Warnings

American Red Cross First Aid 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 ingredients

Benzalkonium Chloride 0.13%
Lidocaine Hydrochloride 4%

Purpose

First aid antiseptic
Pain Relief

Uses

First aid to help prevent bacterial contamination or skin infections, and temporary relief of pain and itching associated with minor:  cutsscrapes  burns  sunburns  skin irritations.

Warnings

For external use only

Ask a doctor before use if you have

deep or puncture wounds  animal bites serious burns

When using this product

• do not use in or near the eyes
• do not apply over large areas of the body or in large quantities
• do not apply over raw surfaces or blistered areas.

Stop use and ask a doctor if

condition worsens symptoms persist for more than 7 days, or 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 and older:clean the affected area  apply a small amount on the area 1 to 3 times daily.  may be covered with a sterile bandage  if bandaged, let dry first.
• Children under 2 years:ask a doctor.

Other information

Store at room temperature.  Protect from excessive heat.

Inactive ingredients

Water (Aqua), Propylene Glycol, Camphor.

Questions/Comments?

Call toll-free 1-877-879-6999
or email at info@amgbrandsllc.com

Package Labeling:

INGREDIENTS AND APPEARANCE

AMERICAN RED CROSS FIRST AID 
benzalkonium chloride, lidocaine hydrochloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51628-0368
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
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51628-0368-0	88.72 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	05/01/2025

Labeler - MY IMPORTS USA, LLC (195767988)

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