AEROSOL FOAM HAND SANITIZER

AEROSOL FOAM HAND SANITIZER

Drug Labeling and Warnings

Drug Details

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HUBOT HEALTHCARE HAND SANITIZER- ethyl alcohol aerosol, foam 
HUBOT HEALTHCARE LLC.

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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AEROSOL FOAM HAND SANITIZER

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

PRINCIPAL DISPLAY PANEL - 34 g Can Label
HUBOT HEALTHCARE HAND SANITIZER 
ethyl alcohol aerosol, foam
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 72138-490
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL54.7 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
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
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 72138-490-1234 g in 1 CAN; Type 0: Not a Combination Product08/24/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/24/2018
Labeler - HUBOT HEALTHCARE LLC. (081084880)
Registrant - HUBOT HEALTHCARE LLC. (081084880)
Establishment
NameAddressID/FEIBusiness Operations
HUBOT HEALTHCARE LLC.081084880MANUFACTURE(72138-490)

Revised: 1/2019
 
HUBOT HEALTHCARE LLC.


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