HandsOnTM HAND SANITIZING GEL

HandsOn HAND SANITIZER by

Drug Labeling and Warnings

HandsOn HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Right Solutions Corporation, The. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HANDSON HAND SANITIZER- ethyl alcohol gel 
Right Solutions Corporation, The

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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HandsOnTM HAND SANITIZING GEL

Drug Facts

Active ingredient

Ethyl Alcohol 65+% v/v

Purpose

Antiseptic

Uses

For hand washing to decrease bacteria on the skin. Recommended for repeated use.

Warnings

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

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

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 and redness develop and persist for more than 72 hours.

Keep out of reach of children ■ If swallowed, get medical help or contact a Poison Control Center right away.

Directions

■ wet hands thoroughly with product. Briskly rub hands together until dry
■ supervise children under 6 years of age in the use of this product.

Other Information

■ store between 20º-25ºC (68º-77ºF)
■ may discolor certain fabrics.

Inactive ingredients

water, triethanolamine, glycerin, propylene glycol, aloe barbadensis leaf extract, fragrance.

moisturizing with aloe
Kills Harmful Bacteria & Germs

MADE IN CANADA / FABRIQUÉ AU CANADA

DISTRIBUTED BY/ DISTRIBUÉ PAR :
THE RIGHT SOLUTIONS CORPORATION, INC.,
100 DELTA PARK BLVD,
BRAMPTON, ONTARIO L6T 5E7
866.308.1738
www.therightsolutions.net

Packaging

HANDSON HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64855-444
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64855-444-23	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/11/2020	08/15/2022
2	NDC: 64855-444-35	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/11/2020	08/15/2022
3	NDC: 64855-444-10	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/11/2020	08/15/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/11/2020	08/15/2022

Labeler - Right Solutions Corporation, The (203855150)

Establishment
Name	Address	ID/FEI	Business Operations
Right Solutions Corporation, The		203855150	manufacture(64855-444)

Revised: 5/2022

Document Id: dc27af00-5131-4872-ad5b-e43548d5cb2f

34390-5

Set id: 2991a836-bb55-482f-9154-6ae4812aa2fc

Version: 2

Effective Time: 20220518