EUNOS ADVANCED HAND SANITIZER- alcohol gel
YIRONG TRADING (NANJING) CO., LTD

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active Ingredient

Alcohol Denat.70% v/v.

Purpose

Antimicrobial

Uses

Hand sanitizer to help reduce bacteria on the skin that could cause disease.

Warnings

Flammable. Keep away from fire or flame.

For external use only

When using this product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
avoid using on broken skin.

Stop use and ask a doctor if irritation or rash appears and lasts

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Put enough product in your palm to cover hands and rub hands together briskly until dry.
Children under 6 years of age should be supervised when using this product

Other Information

Store below 105℉(40℃).
May discolor certain fabrics or surfaces.

Inactive ingredients

Aqua, Acrylates Copolymer, Propylene Glycol, Butylene Clycol, Aminomethyl Propanol

Package Label - Principal Display Panel

60 mL Label

100 mL Label

500 mL Label

EUNOS ADVANCED HAND SANITIZER
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:75007-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:75007-001-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2020
2	NDC:75007-001-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2020
3	NDC:75007-001-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	04/09/2020

Labeler - YIRONG TRADING (NANJING) CO., LTD (554529568)