HAND SANITIZER- ethyl alcohol spray

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Ethyl Alcohol 70%

INACTIVE INGREDIENT

Inactive ingredients: Water, Fragrance, Saccharide Isomerate, Citric Acid, Sodium Citrate, Xylitylglucoside, Anhydroxylitol, Xylitol, Glucose, Aloe Barbadensis Leaf Juice

PURPOSE

Purpose: Antiseptic

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.

INDICATIONS & USAGE

For handwashing to decrease bacteria on the skin. Recommended for repeated use when soap and water are not available

WARNINGS

Warnings:

For external use only. Hands.

Flammable. Keep away from heat or flame.

DOSAGE & ADMINISTRATION

Spray on hands and rub thoroughly until dry

Children under 6 years: use under adult supervision

OTHER SAFETY INFORMATION

Other:

Store below 40°C / 104°F

Avoid freezing and excessive heat

Use Non Alcohol Hand Sanitizer for the refill only.

Shelf life: 3 years (Refer to packaging box for MFG/LoT info)

ASK DOCTOR

Stop use and ask a doctor if

irritation or redness develops.

condition persists for more than 72 hours.

PRINCIPAL DISPLAY PANEL

See Label

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87662-101
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
XYLITOL (UNII: VCQ006KQ1E)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
SACCHARIDE ISOMERATE (UNII: W8K377W98I)
CITRIC ACID (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
ANHYDROXYLITOL (UNII: 8XWR7NN42F)
GLUCOSE (UNII: 5SL0G7R0OK)
FRAGRANCE MINT ORC2000774 (UNII: G7LK3FFB99)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87662-101-02	1 in 1 BOX	05/11/2026
1	NDC: 87662-101-01	20 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/11/2026

Labeler - LESSDOTW CO.,LTD. (658837259)

Establishment
Name	Address	ID/FEI	Business Operations
LESSDOTW CO.,LTD.		658837259	manufacture(87662-101) , label(87662-101)