FDA.reportPublic FDA data

SooAe Hand Sanitizing Wipes

Manufacturer
FIRSTCHAM CO., LTD
Effective date
2022-01-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:19:36

Label at a glance#

ProductSooAe Hand Sanitizing Wipes
Active ingredientBenzalkonium Chloride
Label structure10 sections

Indications and uses

■ For hand washing to decrease bacteria on the skin

Dosage and administration

■ Use entire wipe to thoroughly wipe hands, fingers, and wrists ■ To sanitize, use multiple wipes ■ Discard after single use ■ Keep label closed to prevent moisture loss

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water (Aqua), Phenoxyethanol, Glycerin, Sodium benzoate, Polysorbate 20, Disodium EDTA, Citric Acid, Tocopheryl Acetate

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

handwash

WARNINGS

WARNINGS SECTION

For external use only


Do not use
■ If you are allergic to any of the ingredients


When using this product
■ Do not get into eyes. If contact occurs, rinse thoroughly with water


Stop use and ask a doctor if
■ Irritation or rash develops and continues for more than 72 hours


Keep out of reach of children
■ Unless under adult supervision
■ If swallowed, get medical help or contact a Poison Control Center right away

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■ Unless under adult supervision
■ If swallowed, get medical help or contact a Poison Control Center right away

Uses

INDICATIONS & USAGE SECTION

■ For hand washing to decrease bacteria on the skin

Directions

DOSAGE & ADMINISTRATION SECTION

■ Use entire wipe to thoroughly wipe hands, fingers, and wrists
■ To sanitize, use multiple wipes
■ Discard after single use
■ Keep label closed to prevent moisture loss

Other information

OTHER SAFETY INFORMATION

■ Read the directions and warnings before use
■ Avoid freezing and excessive heat

Questions or Comments?

OTC - QUESTIONS SECTION

■ E-mail: cs@dkcos.com
■ Call 1-212-484-2621

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of packetImage of packet

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73923-015073923-0150-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
Benzalkonium ChlorideF5UM2KM3W7ACTIB
Water059QF0KO0RIACT
PhenoxyethanolHIE492ZZ3TIACT
GlycerinPDC6A3C0OXIACT
Sodium benzoateOJ245FE5EUIACT
Polysorbate 207T1F30V5YHIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
3e97abfb-a6b4-4a91-aca6-081a92292906ab7dd5a0-70a8-4b3a-a0e9-bd15060eac1a2022-01-14WarningsExact identifier
spl set id: ab7dd5a0-70a8-4b3a-a0e9-bd15060eac1a

Reported adverse events (FAERS/openFDA)#

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