HUBOT HEALTHCARE HAND SANITIZER- ethyl alcohol aerosol, foam

HUBOT HEALTHCARE HAND SANITIZER by

Drug Labeling and Warnings

HUBOT HEALTHCARE HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by HUBOT HEALTHCARE LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Ethyl Alcohol 62.5% v/v

Purposes

Antiseptic handwash

Uses

for handwashing to decrease bacteria on the skin

Warnings

• For external use only
• Flammable, keep away from fire or flame, heat, sparks, and sources of static discharge
• Contents under pressure. Do not store at temperatures above 120F (48C), puncture or incinerate.
• Operate only with spout pointing down

Do not use

• In eyes

When using this product

• If in eyes, rinse promptly and thoroughly with water
• Discontinue use if irritation and redness develop

Stop use and ask a doctor if skin irritation or redness occur 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

• Spread thoroughly onto hands and rub until dry.

Other Information

• For additional information, see Safety Data Sheets (SDS)
• For emergency medical information in USA and Canada, call 1-888-255-3924
• For emergency medical information worldwide, call +1-813-248-0573

Inactive Ingredients

Water. Hydrofluorocarbon 152A, Isobutane, Emulsifying wax, steareth-20, Sodium Benzoate, Propane, Cetyl Lactate, Sodium Sesquicarbonate

Questions?

Call +1-574-855-2197

PRINCIPAL DISPLAY PANEL - 34 g Can Label

FOAMING
HAND
SANITIZER

antiseptic | rinse-free

Hubot healthcare

INGREDIENTS AND APPEARANCE

HUBOT HEALTHCARE HAND SANITIZER 
ethyl alcohol aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72138-490
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	54.7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
ISOBUTANE (UNII: BXR49TP611)
STEARETH-20 (UNII: L0Q8IK9E08)
SODIUM BENZOATE (UNII: OJ245FE5EU)
PROPANE (UNII: T75W9911L6)
CETYL LACTATE (UNII: A7EVH2RK4O)
SODIUM SESQUICARBONATE (UNII: Y1X815621J)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72138-490-12	34 g in 1 CAN; Type 0: Not a Combination Product	08/24/2018
2	NDC: 72138-490-08	227 g in 1 CAN; Type 0: Not a Combination Product	03/20/2020
3	NDC: 72138-490-15	425 g in 1 CAN; Type 0: Not a Combination Product	03/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/24/2018

Labeler - HUBOT HEALTHCARE LLC. (081084880)

Registrant - HUBOT HEALTHCARE LLC. (081084880)

Establishment
Name	Address	ID/FEI	Business Operations
HUBOT HEALTHCARE LLC.		081084880	MANUFACTURE(72138-490)