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Strawberry Champagne Hand Sanitizer

Dosage form: liquid
Ingredients: ALCOHOL 62g in 100g
Labeler: Unique Holding Group Inc
NDC Code: 25225-017

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%                               Sanitizer


To decrease bacteria on the skin that could cause diseases

Recommended for repeated use


For external use only-hands. Use only as directed.  Excessive use or prolonged exposure may cause irritation to skin. Discontinue use if rash, redness, or itching occurs.

Flammable. Keep away from heat and flame.

    When using this product

  • Keep out of eyes. In case of contacting with eyes, immediately flash with water and call a doctor.
  • Avoid contacting with a broken skin.

Stop using and ask a doctor if irritation or redness develops.

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.


Put a thumb size amount in your palm and rub hands together briskly until dry.

        Other Information

  • Do not store in temperatures over 118F
  • Children under six years of age should be supervise while using this product.
  • May discolor certain fabrics.

Inactive Ingredients

aloe barbadensis gel, carbomer, deionized water, Fragrance, glycerin, propylene glycol, triethanolamine, and vitamin E


alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:25225-017(NDC:None)
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
Water35.600 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
ALPHA-TOCOPHEROL0.01 g  in 100 g
TROLAMINE0.35 g  in 100 g
STRAWBERRY0.2 g  in 100 g
#Item CodePackage Description
1NDC:25225-017-0130 g in 1 BOTTLE, PLASTIC
2NDC:25225-017-0259 g in 1 BOTTLE, PLASTIC
3NDC:25225-017-04237 g in 1 BOTTLE, PLASTIC
4NDC:25225-017-05500 g in 1 BOTTLE, PLASTIC
5NDC:25225-017-03222 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33307/13/2010
Labeler - Unique Holding Group Inc (529047265)
Registrant - Unique Holding Group Inc (529047265)
Unique Holding Group Inc529047265manufacture

Revised: 07/2010
Unique Holding Group Inc

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.