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aurafresh instant hand sanitizer with moisturizers aloe vera and moisturizers

Dosage form: gel
Ingredients: alcohol 62mL in 100mL
Labeler: Ningbo Pulisi Daily Chemical Products Co., Ltd.
NDC Code: 40104-282

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%      ...        Antiseptic

Hand sanitizer to help decrease bacteria on the skin.

If swallowed, get medical help or contact local poison control center right away.

Children must be supervised in use of this product.

keep out of eyes

when water, soap and towel are not available

For external use only.
Flammable. Keep away from hear or flame.

Do not apply around eyes; Do not use in ears and mouth. When using this products, avoid contact with eyes. In case of contact, flush eyes with water.

Stop using and ask a doctor, if irritation and redness develops, if condition persists for more than 72 hours, consult a doctor.

Pump as needed into your palms and thoroughly spread on both hands, and rub the skin until dry.

Water, Carbomer, Glycerin, Propylene Glycol, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Fragrance

AURAFRESH INSTANT HAND SANITIZER WITH MOISTURIZERS  ALOE VERA AND MOISTURIZERS
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:40104-282
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
alcohol (ALCOHOL) alcohol62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
PROPYLENE GLYCOL 
ALOE VERA LEAF 
CARBOMER 934 
GLYCERIN 
.ALPHA.-TOCOPHEROL ACETATE, D- 
TROLAMINE 
FD&C BLUE NO. 1 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage Description
1NDC:40104-282-01237 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/10/2017
Labeler - Ningbo Pulisi Daily Chemical Products Co., Ltd. (529047265)
Registrant - Ningbo Pulisi Daily Chemical Products Co., Ltd. (529047265)
Establishment
NameAddressID/FEIOperations
Ningbo Pulisi Daily Chemical Products Co., Ltd.529047265manufacture(40104-282)

 
Ningbo Pulisi Daily Chemical Products Co., Ltd.

Medically reviewed on Aug 10, 2017

Further information

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

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