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Instant Hand Sanitizer by Global Protection USA, Inc.

Dosage form: gel
Ingredients: Alcohol 60g in 1mL
Labeler: Global Protection USA, Inc.
NDC Code: 50225-355

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.

Instant Hand Sanitizer

Drug Facts

Active Ingredient

Ethyl Alcohol 66.5%

Purpose

Antiseptic

Uses
  • for handwashing to decrease bacteria on skin without soap and water
  • recommended for repeated use

Warnings

For external use only

Flammable, keep away from fire or flame

Do not use in the eyes. If this happens, rinse thoroughly with water

Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours

Keep out of reach of children

If ingested get medical help or contact a Poison Control Center right away

Directions
  • wet hands thoroughly with product
  • allow to dry without wiping
  • children under 6 should be supervised while using this product

Inactive ingredients aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine

Distributed by
Global Protection USA, Inc.
West Berlin, NJ 08091
800-957-8955

PACKAGE LABEL - PRINCIPAL DISPLAY PANEL – BOTTLE

Global Protection, Inc. “Provider of Homeland Security Equipment”

Instant Hand Sanitizer

Kills 99.9% of Germs

Enriched with Aloe Vera

2 Fl. oz. (59ML)

INSTANT HAND SANITIZER 
instant hand sanitizer gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50225-355
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (Alcohol) Alcohol60 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Aloe 
D&C Green no. 5 
D&C Yellow no. 10 
water 
Product Characteristics
Colorgreen (green) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:50225-355-0159 mL in 1 BOTTLE
2NDC:50225-355-02236 mL in 1 BOTTLE
3NDC:50225-355-03473 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33301/06/2010
Labeler - Global Protection USA, Inc. (030123488)
Registrant - Safetec of America, Inc. (874965262)
Establishment
NameAddressID/FEIOperations
Safetec of America, Inc.874965262MANUFACTURE

 
Global Protection USA, Inc.

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Medically reviewed on Jan 8, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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