FDA.reportPublic FDA data

85989-008-01

Manufacturer
Hangzhou Yida Technology Co., Ltd.
Effective date
2026-05-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:58:42

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

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

WARNINGS SECTION

For external use only

DOSAGE & ADMINISTRATION SECTION

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

INDICATIONS & USAGE SECTION

wet hands thoroughly with wipe • allow to dry without rinsing

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

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		1-1labeling .jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85989-008-01ACTIVE WIPES3 g in 1 PATCHPATCH31
85989-008-01ACTIVE WIPES1500 in 1 BAGPATCH15001

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
85989-00885989-008-01

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
EDETATE DISODIUM7FLD91C86KIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
SODIUM BENZOATEOJ245FE5EUIACT
ALCOHOL3K9958V90MIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
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
ACTIVE WIPESBENZALKONIUM CHLORIDEHangzhou Yida Technology Co., Ltd.52b0f451-343d-9d4d-e063-6294a90ad5e22026-05-25WarningsExact identifier
ndc (package): 85989-008-01
ndc (product): 85989-008
ndc11 (package): 85989000801
spl id: 52b0f451-343e-9d4d-e063-6294a90ad5e2
spl set id: 52b0f451-343d-9d4d-e063-6294a90ad5e2

Reported adverse events (FAERS/openFDA)#

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