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Instant Hand Sanitizer by Unique Holding Group Inc

Medically reviewed on May 7, 2018

Dosage form: liquid
Ingredients: ALCOHOL 62g in 100g
Labeler: Unique Holding Group Inc
NDC Code: 25225-015

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.

Drug Facts

Active Ingredient                                 Purpose

Ethyl Alcohol 62% w/w                       Antiseptic      

Uses:

Hand sanitizer to help decrease bacteria on the skin that could cause diseases



Warnings:

Flammable. Keep away from fore or flame.

For external use only-hands.

 When using this product, do not use in or near the eyes.  In case of contact, rinse eyes thoroughly with water.

Stop use and ask a physician if irritation or skin rash develops.

Keep out of reach of children

if accidentally ingested, seek medical help or contact a Poison Control Center immediately.


    Directions

  •   Place enough product in your palm to thoroughly cover your hands
  • rub hands briskly together until dry
  • children under 6 years of age should be supervised when using this product

        Other Information

  • Store below 105F  
  • May discolor certain fabrics.
  • Maybe harmful to wood finishes and plastics

Inactive Ingredients:

carbomer, fragrance, glycerin, triethanolamine, propylene glycol, deionized water, aloe barbadensis gel

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INSTANT HAND SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:25225-015(NDC:None)
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL62 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Water35.6 g  in 100 g
Propylene Glycol 0.5 g  in 100 g
Glycerin1 g  in 100 g
ALOE VERA LEAF0.01 g  in 100 g
CARBOMER HOMOPOLYMER TYPE C0.33 g  in 100 g
ALPHA-TOCOPHEROL0.01 g  in 100 g
TROLAMINE0.35 g  in 100 g
Packaging
#Item CodePackage Description
1NDC:25225-015-0130 g in 1 BOTTLE, PLASTIC
2NDC:25225-015-0260 g in 1 BOTTLE, PLASTIC
3NDC:25225-015-04237 g in 1 BOTTLE, PLASTIC
4NDC:25225-015-05500 g in 1 BOTTLE, PLASTIC
5NDC:25225-015-03222 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33305/05/2010
Labeler - Unique Holding Group Inc (529047265)
Registrant - Unique Holding Group Inc (529047265)
Establishment
NameAddressID/FEIOperations
Unique Holding Group Inc529047265manufacture

 
Unique Holding Group Inc

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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