AMERICAN RED CROSS ANTISEPTIC CLEANSING FOAM

Manufacturer
Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Effective date
2026-02-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:43:50

Label at a glance#

ProductAMERICAN RED CROSS ANTISEPTIC CLEANSING FOAM
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

first aid to help prevent the risk of bacterial contamination or skin infection associated with 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

protect from freezing or excessive heat store at room temperature.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Cl 0.13% v/v

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warning

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

Do not use :

  • in or near the eyes
  • over large areas of the body or in large quantities
  • longer than 1 week

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have:

  • deep or puncture wounds
  • animal bites
  • serious burns

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 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

  • protect from freezing or excessive heat
  • store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Auqa)

COCAMIDOPROPYL BETAINE

LAURAMINE OXIDE

C10-16 ALKYL GLUCOSIDE

LAURETH-9

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN2
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD2
1020365benzalkonium chloride 0.13 % Topical FoamSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
2d2ef081-4f0c-4669-81e8-32b263669a0aProduct name120230801
af534dc0-c9e5-19a6-693c-e7ad53714660Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75742-082-01AMERICAN RED CROSS ANTISEPTIC CLEANSING FOAM177 mL in 1 BOTTLELIQUID1772

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
75742-08275742-082-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
AMERICAN RED CROSS ANTISEPTIC CLEANSING FOAMBENZALKONIUM CL 0.13% V/VZhejiang Guoyao Jingyue Aerosol Co., Ltd.49e31509-d489-44be-e063-6394a90a97ef2026-02-10WarningsExact identifier
ndc (package): 75742-082-01
ndc (product): 75742-082
ndc11 (package): 75742008201
spl id: 4a8335bb-4f86-d0ff-e063-6294a90ae377
spl set id: 49e31509-d489-44be-e063-6394a90a97ef

Reported adverse events (FAERS/openFDA)#

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