YOOLOGY ALCOHOL-FREE HAND SANITIZER- benzalkonium chloride cream

YOOLOGY Alcohol-Free HAND SANITIZER by

Drug Labeling and Warnings

YOOLOGY Alcohol-Free HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by WHAIN COSMETIC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.066w/w%

Directions

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

For exteral use only.

Stop use and ask a doctor

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

Do not use

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

Keep out of reach of children

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

When using this product

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

Use

Disinfection of hands

Other information

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

Inactive Ingredients

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

Antiseptic

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

YOOLOGY ALCOHOL-FREE HAND SANITIZER 
benzalkonium chloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73823-051
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.033 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CHLORPHENESIN (UNII: I670DAL4SZ)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
PURSLANE (UNII: M6S840WXG5)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHICONE (UNII: 92RU3N3Y1O)
WATER (UNII: 059QF0KO0R)
MINERAL OIL (UNII: T5L8T28FGP)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALLANTOIN (UNII: 344S277G0Z)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
PEG-100 STEARATE (UNII: YD01N1999R)
POLYSORBATE 60 (UNII: CAL22UVI4M)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73823-051-01	50 mL in 1 TUBE; Type 0: Not a Combination Product	07/13/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/13/2021

Labeler - WHAIN COSMETIC (557837595)

Establishment
Name	Address	ID/FEI	Business Operations
WHAIN COSMETIC		695520590	manufacture(73823-051)