FDA.reportPublic FDA data

American Red Cross First Aid Spray

Manufacturer
MY IMPORTS USA, LLC | KOZMO KIMYA SANAYI VE DIS TICARET LIMITED SIRKETI CORLU SUBESI
Effective date
2026-09-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-25 02:01:29

Label at a glance#

ProductAmerican Red Cross First Aid
Active ingredientBENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE
Label structure8 sections

Indications and uses

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

Dosage and administration

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.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%
Lidocaine Hydrochloride 4%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic
Pain Relief

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

• deep or puncture wounds • animal bites • serious burns

When using this product

OTC - WHEN USING SECTION

  • 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

OTC - STOP USE SECTION

• 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

SPL UNCLASSIFIED SECTION

Store at room temperature. • Protect from excessive heat.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Propylene Glycol, Camphor.

Questions/Comments?

OTC - QUESTIONS SECTION

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

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label0Label0

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850052546694GTIN-13: 0850052546694
EAN-13: 0850052546694
GTIN-12: 850052546694
UPC-A: 850052546694
GTIN storage (14 digits): 00850052546694		Label0.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51628-036851628-0368-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-05-01full-release2026-06-01 01:00:14

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
34157041-22de-3e61-e063-6394a90aa5c2667ab8ce-e110-4b7f-a158-3cdd3b7a1c292025-05-01WarningsExact identifier
spl set id: 667ab8ce-e110-4b7f-a158-3cdd3b7a1c29

Reported adverse events (FAERS/openFDA)#

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