CLEAN CARE HAND SANITIZER- alcohol gel 
URBANBCL CO LTD

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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Drug Facts

ethyl alcohol

The convenient Sense Fresh Advanced Instant Hand Sanitizer with Aloe is an antimicrobial liquid that contains 70 percent ethyl alcohol to help reduce the number of germs on hands, and three moisturizers to help keep skin hydrated. No rinsing with water or drying with towels is needed. Alcohol-based hand sanitizers can quickly reduce the number of germs on hands within 30 seconds. The hand sanitizer meets U.S. Food and Drug Administration (FDA) healthcare personnel hand-washing requirements. It’s perfect for on-the-go uses when traveling outside of the home, and fits neatly in purses, backpacks or briefcases.

KEEP OUT OF REACH OF THE CHILDREN

Just spray enough product in your palm to cover hands and rub hands together briskly until dry.

Children under 6 years of age should be supervised when using Sense Fresh.

Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

■ Flammable. Keep away from fire or flame.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

for external use only

water, trolamine, dipropylene glycol, carbomer

label

CLEAN CARE HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74200-0002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74200-0002-1500 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2020
2NDC:74200-0002-2100 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/01/2020
Labeler - URBANBCL CO LTD (694794065)
Registrant - URBANBCL CO LTD (694794065)
Establishment
NameAddressID/FEIBusiness Operations
URBANBCL CO LTD694794065manufacture(74200-0002)

Revised: 4/2020
Document Id: a24d1053-11c9-ef44-e053-2995a90a6b77
Set id: a24d1fc5-447f-29c3-e053-2a95a90a43af
Version: 1
Effective Time: 20200402
 
URBANBCL CO LTD