Hyatt Hand Sanitizer 70% Alcohol

Hyatt Hand Sanitizer 70% Alcohol by

Drug Labeling and Warnings

Hyatt Hand Sanitizer 70% Alcohol by is a Otc medication manufactured, distributed, or labeled by Hunter Amenities International Limited, KIMIRICA HUNTER INTERNATIONAL LLP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HYATT HAND SANITIZER 70% ALCOHOL- alcohol gel 
Hunter Amenities International Limited

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.

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Hyatt Hand Sanitizer 70% Alcohol

Drug Facts

Active ingredient (v/v)

Ethyl Alcohol 70.0 %

Purpose

Antiseptic skin cleanser

Uses

  • Antiseptic (skin) cleanser
  • Medicated (skin) cleanser
  • Antibacterial (skin) cleanser
  • Kills harmful bacteria/germs
  • Effective in destroying (harmful) bacteria to provide antiseptic cleansing
  • For perosnal hand hygine to help prevent the spread of bacteria

Warnings

For external use only.

When using this product

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask/ consult a doctor/ physician/ health care practitioner/ health care provider/ health care professional if

irritation develops.

Keep out of reach of children.

if swallowed, call a Poison Control Center or get medical help right away.

Flammability warning.

Keep away from open flame and sources of heat.

Directions

Adults and children over 2 years:

  • For occasional and personal domestic use.
  • Supervise children when they use this product.
  • Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Inactive ingredients

Aqua/Water/Eau, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Aloe Barbadensis Leaf Extract, Avena Sativa Kernal Extract, PEG-40 Hydrogenated Castor Oil, Tocopherol Acetate.

Questions?

1-800-668-1483

Package Labeling:

Bottle

HYATT HAND SANITIZER 70% ALCOHOL 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 65910-015
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
TROLAMINE (UNII: 9O3K93S3TK)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 65910-015-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/202007/31/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/01/202007/31/2022
Labeler - Hunter Amenities International Limited (244071015)
Establishment
NameAddressID/FEIBusiness Operations
KIMIRICA HUNTER INTERNATIONAL LLP856827349manufacture(65910-015)

Revised: 9/2022
Document Id: e8064928-0f7b-04b4-e053-2a95a90a974c
Set id: 9ba0a549-2143-4723-811e-e62d7fb93127
Version: 4
Effective Time: 20220906