MR. HAND SANITIZER- alcohol liquid

Mr. Hand Sanitizer by

Drug Labeling and Warnings

Mr. Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by MR. HAND, LLC, Pure Source, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

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

Warnings

Flammable. Keep away from fire or flame.

For external use only.

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash occurs.

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.

DO NOT USE

Do Not Use

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

Directions

• Place enough product in your palm to thoroughly cover your hands.
• Rub hands briskly until they are fully dry.

Other Information

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

Inactive Ingredients

Water, hydrolized jojoba esters, glycerin, PEG-10 dimethicone, sodium hyaluronate, cannabidiol.

PRINCIPAL DISPLAY PANEL

Mr. Hand Sanitizer

CBD Infused

5.7 fl. oz /168 ml

INGREDIENTS AND APPEARANCE

MR. HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79283-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
WATER (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL 500 (UNII: 761NX2Q08Y)
DIMETHICONE (UNII: 92RU3N3Y1O)
JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
CANNABIDIOL (UNII: 19GBJ60SN5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79283-001-01	168 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/18/2020

Labeler - MR. HAND, LLC (117563109)

Establishment
Name	Address	ID/FEI	Business Operations
Pure Source, LLC		080354456	manufacture(79283-001)