SaniStationTM HAND SANITIZING GEL

SaniStation HAND SANITIZING by

Drug Labeling and Warnings

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

Drug Details [pdf]

SANISTATION HAND SANITIZING- 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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SaniStationTM HAND SANITIZING GEL

Drug Facts

Active ingredient

Ethyl Alcohol 70% 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.

STOP THE SPREAD OF GERMS

MOISTURZING WITH ALOE

KILLS HARMFUL BACTERIA & GERMS

MADE IN CANADA 

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

Packaging

SANISTATION HAND SANITIZING 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64855-445
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
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: 64855-445-23	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/2020	08/15/2022
2	NDC: 64855-445-35	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/2020	08/15/2022
3	NDC: 64855-445-71	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/2020	08/15/2022

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

Labeler - Right Solutions Corporation, The (203855150)

Establishment
Name	Address	ID/FEI	Business Operations
Right Solutions Corporation, The		203855150	manufacture(64855-445)

Revised: 5/2022

Document Id: e8d5a3d7-bf16-4899-9fe5-7d20bfa7a6bc

34390-5

Set id: 8b329065-81b1-4894-ac8a-31f81c2c759e

Version: 2

Effective Time: 20220518