EUNOS ADVANCED HAND SANITIZER- alcohol gel

EUNOS ADVANCED HAND SANITIZER by

Drug Labeling and Warnings

EUNOS ADVANCED HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by YIRONG TRADING (NANJING) CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 75% v/v.

Purpose

Antimicrobial

Use

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

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 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

Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Aminomethyl Propanol, Aloe Barbadensis (Aloe Vera) Gel, Tocopheryl Acetate (Vitamin E)

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

EUNOS ADVANCED HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75007-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75007-004-01	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
2	NDC: 75007-004-02	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
3	NDC: 75007-004-03	119 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
4	NDC: 75007-004-04	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
5	NDC: 75007-004-05	474 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
6	NDC: 75007-004-06	947 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020

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