ASSORTED LICENSED HAND SANITIZER VANILLA 01- alcohol spray

Assorted Licensed Hand Sanitizer Vanilla by

Drug Labeling and Warnings

Assorted Licensed Hand Sanitizer Vanilla by is a Otc medication manufactured, distributed, or labeled by Shenzhen Lantern Scicence Co.,Ltd., Shenzhen Lantern Science Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

drug facts

Active Ingredient

Active ingredient Purpose

Ethyl Alcohol 70% v/v Antiseptic

Uses

Decreases bacieria on skin

Warning

For external use only

Do not use

lf you are allergic to any of the ingredients

When using this product

Do not get into eyes. lf contact occurs, rinse thoroughly with water.Do not use in or near eyes,In case of eye contact ,flush eyes thoroughly with water. Discontinue if skin becomes irritated and ask for a doctor.

Stop use and ask a doctor

lf irritation or rash develops and continues for more than72 hours.

keep out of reach of children

lf swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Adults and children 6 years and older
Spray onto hands and rub together unil dry. Recommended for repeat use.
Children under 6 years of age
should be supervised when using this product.

Inactive ingredients

Water, Fragrance,Glycerin, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, Aminomethyl Propanol, Tocopheryl Acetate, Aloe Barbadensis Gel, Denatonium Benzoate.

other Information

Storebetween15-30C(59-86F)
Avoid freezing and excessive heat above 40C (104F)

DOSAGE & ADMINISTRATION

Spray 3-4 times each time.
Used in the skin area of the hands.

packing

packing

INGREDIENTS AND APPEARANCE

ASSORTED LICENSED HAND SANITIZER VANILLA  01
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54860-425
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54860-425-01	28 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/06/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	07/06/2024

Labeler - Shenzhen Lantern Scicence Co.,Ltd. (421222423)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Lantern Science Co.,Ltd.		421222423	manufacture(54860-425)