HELLO HAND SANITIZER - ALOE AND SEA MINERALS- alcohol spray

Hello hand sanitizer - aloe and sea minerals by

Drug Labeling and Warnings

Hello hand sanitizer - aloe and sea minerals by is a Otc medication manufactured, distributed, or labeled by Hello Products LLC, MYKU Biosciences LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s) Purpose

Ethyl Alcohol 62%...............................................Antiseptic

Use(s)

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. Do not spray towards face. Flammable. Keep away from heat or flame.

Stop use and ask a doctor

if irritation or rash occurs.

Do not use

in children less than 2 months of age or 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.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

DOSAGE & ADMINISTRATION

Inactive ingredients

Water, Triethyl Citrate, Sodium L-pyroglutamate, Fragrance, Aloe Vera Juice, Mixed Tocopherols, Potassium Sorbate, Sodium Benzoate

OTHER SAFETY INFORMATION

Other Information

• Store between 15-30ºC (59-86ºF)
• Avoid freezing and excessive heat above 40ºC (104ºF)

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HELLO HAND SANITIZER - ALOE AND SEA MINERALS 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55882-6111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
TOCOPHEROL (UNII: R0ZB2556P8)
SODIUM PIDOLATE (UNII: 1V74VH163T)
WATER (UNII: 059QF0KO0R)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55882-6111-2	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/01/2020

Labeler - Hello Products LLC (040714890)

Registrant - MYKU Biosciences LLC (106728135)

Establishment
Name	Address	ID/FEI	Business Operations
MYKU Biosciences LLC		106728135	manufacture(55882-6111)