MAYO HYGIENE INSTANT HAND SANITIZER- alcohol gel
Zhejiang Cuifu Cosmetics 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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Mayo Hygiene Instant Hand Sanitizer

Drug Facts

Active ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

A Hand Sanitizer to help reduce bacteria that potentially can cause disease. Recommended for repeated use. For use when soap and water are not available.

Warnings

For external use only.

Flammable. Keep away from heat or flame.

When using this product

do not use in or near eyes,ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or rash appears on the skin.

Keep out of reach of children.

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

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Children under 6 years of age should be supervised by adult when applying this product.
Do not use on children less than 2 months of age or on open skin wounds.

Other information

Do not store above 40C(104F). May discolor some fabrics or surfaces.

Inactive ingredients

Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Carbomer, Glycerin, Water.

Package Labeling:

Bottle

MAYO HYGIENE INSTANT HAND SANITIZER
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:75809-000
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL in 1 mL

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:75809-000-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	06/13/2020

Labeler - Zhejiang Cuifu Cosmetics Co., Ltd (554531268)