HAND SANITIZER- ethyl alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by MINISO DEPOT CA, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient
Ethyl Alcohol 62%

PURPOSE

Purpose
Antiseptic

INDICATIONS & USAGE

Uses Decrease bacteria on hands

WARNINGS

Warnings For external use only.

Keep out of eyes. In case of contact with eyes, flush

KEEP OUT OF REACH OF CHILDREN

Keep it out of reach of children.

STOP USE

Stop use and ask a doctor if irritation or redness develop.If swallowed,get medical help or contact a doctor right away.

STORAGE AND HANDLING

Storage: Flammable,Avoid direct sunlight and keep away from fire.

DOSAGE & ADMINISTRATION

Directions: Wet hands thoroughly with product and allow to dry without wiping.

INACTIVE INGREDIENT

Inactive Ingredients:

Water (Aqua),Glycerin, Propylene Glycol,Fragrance (Parfum), Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Lactose, Microcrystalline Cellulose, Sucrose, Zea Mays(Corn)Starch, Tocopheryl Acetate, Hydroxypropyl Methylcellulose, Aloe Barbadensis Leaf Juice, Maltodextrin,Benzyl Salicylate, Citronellol, Eugenol, Geraniol, Linalool, Ultramarines (CI77007), FD&C Red No.4 (CI14700), D&C Red No.33 (CI17200)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73950-001
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
GERANIOL (UNII: L837108USY)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
ULTRAMARINE BLUE (UNII: I39WR998BI)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
.ALPHA.-LACTOSE (UNII: MJF4JAT10B)
SUCROSE (UNII: C151H8M554)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
STARCH, CORN (UNII: O8232NY3SJ)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
EUGENOL (UNII: 3T8H1794QW)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73950-001-01	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/23/2020

Labeler - MINISO DEPOT CA, INC. (056958961)