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GELRITE

Medically reviewed on April 5, 2018

Dosage form: gel
Ingredients: ALCOHOL 65mL in 100mL
Labeler: DERMARITE INDUSTRIES, LLC
NDC Code: 61924-106

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.

GELRITE

Active Ingredient

Alcohol 65%

Purpose

Antiseptic

​Uses
  • For handwashing to decrease bacteria on skin.
  • Recommended for repeated use.

​Warnings

For external use only.

​Flammable. Keep away from heat and flame.

Avoid contact with eyes. ​In case of contact, flush thoroughly with water.

Stop use and ask a doctor if skin irritation develops.

.

Directions
  • ​Wet hands thoroughly with product and allow to dry without wiping.
  • Children under six should be supervised while using this product.

Other Information
  • Do not store above 105°F
  • May discolor some fabrics or surfaces
  • You may report a serious adverse event to DermaRite Industries, PO Box 7209, North Bergen, NJ 07047

​Inactive ingredients

Water, Propylene Glycol, Carbomer, Polysorbate 20, Fragrance, t-Butanol, Triethanolamine, Tocopherol Acetate, Sodium Isostearoyl Lactate, Denatonium Benzoate

Questions?

Call 1-800-337-6296 Mon-Fri 9AM-5PM EST.

Keep out of reach of children

Keep out of reach of children. ​In case of accidental ingestion contact a physician or Poison Control Center right away

GelRite Package Label Principal Display Panel

GELRITE 
hand sanitizer gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61924-106
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL65 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CARBOMER 940 
DENATONIUM BENZOATE ANHYDROUS 
PROPYLENE GLYCOL 1,2-DISTEARATE 
BUTANOL (MIXED ISOMERS) 
2,4,5-T-TROLAMINE 
.ALPHA.-TOCOPHEROL ACETATE 
SODIUM ISOSTEAROYL LACTYLATE 
Packaging
#Item CodePackage Description
1NDC:61924-106-04118 mL in 1 BOTTLE, DISPENSING
2NDC:61924-106-16473 mL in 1 BOTTLE, PUMP
3NDC:61924-106-27800 mL in 1 BAG
4NDC:61924-106-341000 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/25/2006
Labeler - DERMARITE INDUSTRIES, LLC (883925562)
Registrant - DERMARITE INDUSTRIES, LLC (883925562)
Establishment
NameAddressID/FEIOperations
DERMARITE INDUSTRIES LLC883925562manufacture(61924-106)

 
DERMARITE INDUSTRIES, LLC

Further information

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

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