QUR EUCALYPTUS ESSENTIAL OIL HAND SANITIZER- alcohol gel

QUR Eucalyptus Essential Oil Hand Sanitizer by

Drug Labeling and Warnings

QUR Eucalyptus Essential Oil Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by K7 Design Group Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Alcohol 69% v/v

Purpose

Antiseptic

Use

for hand-washing to decrease bacteria on the skin, only when water is not available

Warnings

Flammable, keep away from fire and flames

For external use only

When using this product

• do not get into eyes.
• if contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

• irritation and redness develop

Keep out of reach of children.

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

Directions

• wet hands thoroughly with product and allow to dry without wiping

Inactive ingredients

Water, Glycerin, Propylene Glycol, Carbomer, Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Tocopheryl Acetate, Eucalyptus Citriodora Leaf Extract, Denatonium Benzoate.

Company Information

MANUFACTURED FOR & DISTRIBUTED BY QUR

NEW YORK, NY 10128

Product Packaging

INGREDIENTS AND APPEARANCE

QUR EUCALYPTUS ESSENTIAL OIL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74177-992
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	69 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CORYMBIA CITRIODORA LEAF OIL (UNII: M63U6N96EB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74177-992-01	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/19/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/19/2021

Labeler - K7 Design Group Inc. (080357784)