HAND SANITIZER- alcohol gel 
Jubilant, LLC

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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Advanced Hand Sanitizer

Active Ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

Warnings

For external use only-hands

Flammable.  Keep away from heat and flame.

When using this product

Stop use and ask a doctor if

Keep out of reach of children.

If swallowed get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

water, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4

*Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds

DISTRIBUTED BY: Jubilant LLC

451 Broadway, F12

New York, NY 10013

www.princeSpring.com

Pat. 9,161,982

SDS-MO-15036

SDA-WI-2486

DSP-MO-28

DSP-MO-34

Questions?  Comments?  732-783-4090

hi@princespring.com

principal display panel

Prince & Spring

Advanced Hand Sanitizer

Moisturizing formula with Vitamin E

Kills more than 99.99% of germs*

Get a hand-le on germs

67.6 FL OZ (2 L)

image description

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71569-370
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
SULISOBENZONE (UNII: 1W6L629B4K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71569-370-882000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/11/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/11/2017
Labeler - Jubilant, LLC (079508724)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(71569-370)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(71569-370)

Revised: 3/2022
Document Id: 3e26cfcc-8cf7-4b64-814b-72c01f218d1e
Set id: d559ff3d-a4a5-4a3d-a489-134760584c95
Version: 12
Effective Time: 20220303
 
Jubilant, LLC