SWEET ORANGE BERGAMOT AND ALOE- ethyl alcohol gel

Sweet Orange Bergamot and Aloe by

Drug Labeling and Warnings

Sweet Orange Bergamot and Aloe by is a Otc medication manufactured, distributed, or labeled by ALO New York LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Ethyl Alcohol

Purpose

Antiseptic

Uses

For handwashing to decrease bacteria on the skin

Warnings

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

When using this product

Do not use in eyes. In case of contact with eyes, rinse with water.

Stop use and ask doctor if

irritation and redness develop and persist.

Keep out of reach of chidren.

If swallowed, get medical help promptly.

Directions

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

Other information

Store under 105°F

Inactive Ingredients

Water, Glycerine, Rapidgel EZ, Aloe Barbadensis Leaf, Citrus Aurantium Dulcis (Sweet Orange) Oil, Citrus Aurantium Bergamia (Bergamot)Oil

PRINCIPAL DISPLAY PANEL

NDC: 82355-002-08

ALOH Sanitizing Hand Gel

Sweet Orange Bergamot + Aloe

70 Percent Alcohol

8 fl oz

INGREDIENTS AND APPEARANCE

SWEET ORANGE BERGAMOT AND ALOE 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82355-002
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
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
RAPIDGEL EZ1 (UNII: 33JH4A7R2K)
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)
ORANGE OIL, COLD PRESSED (UNII: AKN3KSD11B)
CITRUS AURANTIUM BERGAMIA (BERGAMOT) LEAF OIL (UNII: ZVY8741I1V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82355-002-08	238 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/02/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	04/02/2025

Labeler - ALO New York LLC (110122374)

Registrant - ALO New York LLC (110122374)