AMORAY PREMIUM INSTANT HAND SANITIZER WITH ALOE AND VITAMIN E ORIGINAL- alcohol gel

amoray premium instant hand sanitizer with aloe and vitamin e by

Drug Labeling and Warnings

amoray premium instant hand sanitizer with aloe and vitamin e by is a Otc medication manufactured, distributed, or labeled by NINGBO SANTE YING MEDICALAND HEALTHDEVELOPMENT CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                  Purpose

Ethyl Alcohol                62%      ...        Antimicrobial

PURPOSE

Hand sanitizer to help decrease bacteria on the skin that may cause disease.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact local poison control center right away.

Children must be supervised in use of this product.

INDICATIONS & USAGE

keep out of eyes

when water, soap and towel are not available

WARNINGS

For external use only.
Flammable. Keep away from hear or flame.

Do not apply around eyes; Do not use in ears and mouth. When using this products, avoid contact with eyes. In case of contact, flush eyes with water.

Stop using and ask a doctor, if irritation and redness develops, if condition persists for more than 72 hours, consult a doctor.

DOSAGE & ADMINISTRATION

Pump as needed into your palms and thoroughly spread on both hands, and rub the skin until dry. 

Children under 6 years of age should be supervised by an adult when using.

INACTIVE INGREDIENT

Water, Carbomer, Glycerin, Propylene Glycol, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E), Fragrance

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AMORAY PREMIUM INSTANT HAND SANITIZER WITH ALOE AND VITAMIN E  ORIGINAL
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73344-108
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	alcohol	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER 934 (UNII: Z135WT9208)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73344-108-01	53 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/29/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/29/2019

Labeler - NINGBO SANTE YING MEDICALAND HEALTHDEVELOPMENT CO.,LTD (404080257)

Registrant - NINGBO SANTE YING MEDICALAND HEALTHDEVELOPMENT CO.,LTD (404080257)

Establishment
Name	Address	ID/FEI	Business Operations
NINGBO SANTE YING MEDICALAND HEALTHDEVELOPMENT CO.,LTD		404080257	manufacture(73344-108)