FDA.reportPublic FDA data

AIWINA Sanitizing Wet Wipes

Manufacturer
HONGKONG YIFAR INDUSTRIAL LIMITED
Effective date
2020-06-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:19:33

Label at a glance#

ProductAIWINA Sanitizing Wet Wipes
Active ingredientALCOHOL, BENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

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

Dosage and administration

Wet hands thoroughly with product and allow to dry without rinse. Children under six years of age should be supervised when using this product.

Storage and handling

Store in a dry place away from fire.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0. 10%

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.
Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.
Do not use if you are allergic to any of the ingredients.
Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children unless under adult supervision.
• If swallowed, get medical help.

Directions of use

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry without rinse.
  • Children under six years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

Store in a dry place away from fire.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Glycerol, Propanediol, Aloe Vera Extract, Amino acid moisturizer, Hexadecylpyridinium Chloride, Vitamin E, Citric acid, Sodium citrate, Dodecyl polyglucoside.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2381635benzalkonium chloride 0.1 % / ethanol 75 % Medicated PadPSN1
2381635benzalkonium chloride 1 MG/ML / ethanol 0.75 ML/ML Medicated PadSCD1
2381635benzalkonium chloride 0.1 % / ethanol 75 % Medicated PadSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79011-001-802022-01-28C16284748780-1d6a99b39-dcf0-a426-e053-dadaa90af4c2d17730bc-1cd4-4000-85e4-e3a4eaf3e073

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79011-001-80AIWINA Sanitizing Wet Wipes4.25 mL in 1 PACKETCLOTH4.251
79011-001-80AIWINA Sanitizing Wet Wipes80 in 1 CANISTERCLOTH801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79011-001AIWINA SANITIZING WET WIPES (ALCOHOL, BENZALKONIUM CHLORIDE) CLOTH [HONGKONG YIFAR INDUSTRIAL LIMITED]1Legacy NDC, 2 package rows20200630_d17730bc-1cd4-4000-85e4-e3a4eaf3e073.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79011-00179011-001-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPANEDIOL5965N8W85TIACT
ALOE VERA LEAFZY81Z83H0XIACT
BETAINE3SCV180C9WIACT
CETYLPYRIDINIUM CHLORIDED9OM4SK49PIACT
ALPHA-TOCOPHEROLH4N855PNZ1IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM CITRATE1Q73Q2JULRIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT

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
f4013420-81d3-4336-9672-e8d9223fef9bd17730bc-1cd4-4000-85e4-e3a4eaf3e0732020-06-17WarningsExact identifier
spl id: f4013420-81d3-4336-9672-e8d9223fef9b
spl set id: d17730bc-1cd4-4000-85e4-e3a4eaf3e073

Reported adverse events (FAERS/openFDA)#

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