FDA.reportPublic FDA data

HAND SANITIZING WIPES

Manufacturer
Skaffles Group Limited Liability Company | Zhejiang Qimei Commodity Co.,Ltd.
Effective date
2020-05-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:13:35

Label at a glance#

ProductHAND SANITIZING WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

Directions● Adults and children 2 yrs and over, apply to hands and allow skin to dry without wiping. ●Children under 2, ask doctor before use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.3%

Purpose

OTC - PURPOSE SECTION

Antibacterial

USE

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.
Recommended for repeated use.

Warning

WARNINGS SECTION

For external use only. Do not use if you are allergic to
any of the ingredients.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions● Adults and children 2 yrs and over,
apply to hands and allow skin to dry without wiping.
●Children under 2, ask doctor before use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients Water, Aloe Barbadensis Leaf Juice,
PEG-75 Lanolin, Quatermium-52, PEG-8 Dimethicone, Disodium
Cocoamphodiacetate, Disodium EDTA, Chamomilla Recutita
(Matricaria) Flower Extract, Potassium Sorbate, Phenoxyethanol,
Cetylpyridinium Chloride, Sodium Benzoate, Citric Acid.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1111

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1812737benzalkonium Cl 0.3 % Medicated PadPSN1
1812737benzalkonium chloride 3 MG/ML Medicated PadSCD1
1812737benzalkonium chloride 0.3 % Medicated WipeSY1
1812737benzalkonium chloride 0.3 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77720-001-012022-01-28C16284748780-1d6a99b39-a667-a426-e053-dadaa90af4c277720-001 HAND SANITIZING WIPES 0.3% BENZALKONIUM CHLORIDE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77720-001-01HAND SANITIZING WIPES30 in 1 BAGCLOTH301
77720-001-01HAND SANITIZING WIPES48 in 1 CARTONCLOTH481

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77720-001HAND SANITIZING WIPES (BENZALKONIUM CHLORIDE) CLOTH [SKAFFLES GROUP LIMITED LIABILITY COMPANY]1Legacy NDC, 2 package rows20200519_a5ba7924-cb92-209a-e053-2a95a90a8633.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77720-00177720-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
QUATERNIUM-52588EQF3H1PIACT
PEG-75 LANOLIN09179OX7TBIACT
ALOE VERA LEAFZY81Z83H0XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
CETYLPYRIDINIUM CHLORIDED9OM4SK49PIACT
PEG-8 DIMETHICONEGIA7T764ODIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
DISODIUM EDTA-COPPER6V475AX06UIACT
CHAMOMILEFGL3685T2XIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM BENZOATEOJ245FE5EUIACT

Source Document#

Source XML · Source PDF

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
a5ba78c1-bb6b-ec80-e053-2995a90ab657a5ba7924-cb92-209a-e053-2a95a90a86332020-05-15WarningsExact identifier
spl id: a5ba78c1-bb6b-ec80-e053-2995a90ab657
spl set id: a5ba7924-cb92-209a-e053-2a95a90a8633

Reported adverse events (FAERS/openFDA)#

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