ARUBA ALOE HAND SANITIZER- alcohol cream

Aruba Aloe Hand Sanitizer by

Drug Labeling and Warnings

Aruba Aloe Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Aruba Aloe Balm NV. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Alcohol 80.00% v/v

Purpose

Antiseptic

Uses

• Hand sanitizer to help reduce bacteria that potentially can cause disease.
• For use when soap and water are not available.

Warnings

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

Do not use

• On children less than 2 months of age
• On open skin wounds

When using this product

keep out of 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 occurs. These may be signs of a serious condition.

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.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30°C (59-86°F)
• Avoid freezing and excessive heat above 40°C (104°F)

Inactive Ingredients

Water (Aqua/Eau), Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Juice (Aloe Vera Gel from Aruba), Fragrance (Parfum), Citric Acid.

Package Labeling:

INGREDIENTS AND APPEARANCE

ARUBA ALOE HAND SANITIZER 
alcohol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53675-213
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53675-213-00	59 mL in 1 TUBE; Type 0: Not a Combination Product	06/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/15/2025

Labeler - Aruba Aloe Balm NV (855442273)

Registrant - Aruba Aloe Balm NV (855442273)