YOOLOGY Alcohol-Free HAND SANITIZER

Manufacturer
WHAIN COSMETIC
Effective date
2021-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:41:25

Label at a glance#

ProductYOOLOGY Alcohol-Free HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing. Avoid direct inhalation of vapors during application. (Headaches and irritation to mucous membranes may occur when directly inhaled.) This product is intended only for hand sanitizing. To prevent contents from drying out and contaminants from enteri...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.066w/w%

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing. Avoid direct inhalation of vapors during application. (Headaches and irritation to mucous membranes may occur when directly inhaled.) This product is intended only for hand sanitizing. To prevent contents from drying out and contaminants from entering, close lid completely after use. Do not use over bandages, castings, etc. as irritation may occur.

Warnings

WARNINGS SECTION

For exteral use only.

Stop use and ask a doctor

OTC - ASK DOCTOR SECTION

if irritation or rash occurs. These may be signs of a serious conditon.

Do not use

OTC - DO NOT USE SECTION

  • In children less than 2 months of age
  • On open skin wounds

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears and mouth. In case of contract with eyes, rinse eyes thoroughly with water.

Use

INDICATIONS & USAGE SECTION

Disinfection of hands

Other information

OTHER SAFETY INFORMATION

Store between 15~30ºC(59~86ºF) Avoid freezing and excessive heat above 40ºC (104ºF)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Mineral Oil, Cetearyl Alcohol, GlycerylStearate, Sorbitan Stearate, Polysorbate 60, Microcrystalline Wax, Phenoxyethanol, Chlorphenesin,Dimeticone, Carbomer, Trietanolamine, Caprylic/Capric Triglyceride, Disodium EDTA, Allantoin,Sodium Hyaluronate, Lavendula Angustifolia (Lavender)Extract, Portulaca Oleracea Extract, PEG-100 Stearate, Fragrance

Purpose

OTC - PURPOSE SECTION

Antiseptic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

300 mL300 mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2288822benzalkonium chloride 0.066 % Topical LotionPSN1
2288822benzalkonium chloride 0.66 MG/ML Topical LotionSCD1
2288822benzalkonium chloride 0.066 % Topical LotionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73823-301-012023-01-30C16284748780-1f386c64a-0707-0266-e053-dadaa90a7c1a[WHAIN COSMETIC] [300 mL, Bottle+Pump] YOOLOGY Alcohol-Free HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73823-301-01YOOLOGY Alcohol-Free HAND SANITIZER300 mL in 1 BOTTLE, PUMPCREAM3001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73823-301YOOLOGY ALCOHOL-FREE HAND SANITIZER (BENZALKONIUM CHLORIDE) CREAM [WHAIN COSMETIC]1Legacy NDC, 1 package rows20210713_c57df558-b08e-5197-e053-2a95a90a8d29.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73823-30173823-301-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

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
c57df558-b08f-5197-e053-2a95a90a8d29c57df558-b08e-5197-e053-2a95a90a8d292021-07-13WarningsExact identifier
spl id: c57df558-b08f-5197-e053-2a95a90a8d29
spl set id: c57df558-b08e-5197-e053-2a95a90a8d29

Reported adverse events (FAERS/openFDA)#

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