FDA.reportPublic FDA data

84323-008-01Active Wipes

Manufacturer
Zhejiang StarryApex Biotechnology Co., Ltd.
Effective date
2026-05-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:56:32

Label at a glance#

ProductActive Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13% w/w

OTC - PURPOSE SECTION

Antimicrobial

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

WARNINGS SECTION

For external use only

When using this product
• do not use in or near eyes
• discontinue use if irritation and redness develop

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with wipe • allow to dry without rinsing

INDICATIONS & USAGE SECTION

to sanitize hands without requiring water or a rinse
kills 99.9% of most common germs

INACTIVE INGREDIENT SECTION

Water, SD Alcohol 40, Phenoxyethanol, Decyl Glucoside, Potassium Sorbate, Sodium Benzoate, Disodium EDTA, Citric Acid, Aloe Barbadensis (Aloe) Leaf Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

84323-008-01 labeling84323-008-01 labeling

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN1
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD1
1038558benzalkonium chloride 0.13 % Topical ClothSY1
1038558benzalkonium chloride 0.13 % Topical SwabSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY1
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130634562779717GTIN-13: 0634562779717
EAN-13: 0634562779717
GTIN-12: 634562779717
UPC-A: 634562779717
GTIN storage (14 digits): 00634562779717		1-1.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84323-008-01Active Wipes1500 in 1 BAGPASTE15001
84323-008-01Active Wipes3 g in 1 PACKETPASTE31

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84323-00884323-008-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID2968PHW8QPIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
ALCOHOL3K9958V90MIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
SODIUM BENZOATEOJ245FE5EUIACT
EDETATE DISODIUM7FLD91C86KIACT
ALOE VERA LEAFZY81Z83H0XIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
53bb6d34-04b4-95d8-e063-6294a90af99f514a4ef5-dfcd-c704-e063-6394a90ae4ca2026-06-08WarningsExact identifier
spl set id: 514a4ef5-dfcd-c704-e063-6394a90ae4ca

Reported adverse events (FAERS/openFDA)#

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