HUANGJISOO HAND SANITIZER- alcohol gel 
Newfeel

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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ACTIVE INGREDIENT

Active ingredients: Ethyl Alcohol 62.00%

INACTIVE INGREDIENT

Inactive ingredients:

Water, Glycerin, Carbomer, 1,2-Hexanediol, Apium Graveolens (Celery) Extract, Daucus Carota Sativa (Carrot) Root Extract, Foeniculum Vulgare (Fennel) Seed Extract, Brassica Oleracea Acephala Leaf Extract, Coriandrum Sativum (Coriander) Extract, Lactuca Scariola Sativa (Lettuce) Leaf Extract, Spinacia Oleracea (Spinach) Leaf Extract

PURPOSE

Purpose: Antiseptic

WARNINGS

Warnings:
For external use only : hands
Flammable, keep away from fire or flame.
When using this product ■ keep out of eyes. In case of contact with eyes, flush thoroughly with water. ■ avoid contact with broken skin. ■ do not inhale or ingest
Stop use and ask a doctor if ■irritation and redness develop ■ condition persists for more than 72 hours
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Uses:
■ for handwashing to decrease the bacteria on the skin
■ recommended for repeated use

Directions

Directions: Rub a dime sized drop into hands.

PACKAGE LABEL - 500mL, Bottle

Image of bottle

PACKAGE LABEL - 30mL, Bottle

Image of bottle

HUANGJISOO HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73713-020
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73713-020-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2020
2NDC:73713-020-0230 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/01/2020
Labeler - Newfeel (690062383)
Registrant - Newfeel (690062383)
Establishment
NameAddressID/FEIBusiness Operations
Newfeel690062383manufacture(73713-020)

Revised: 3/2020
Document Id: 05e37286-8f8b-4438-bcd4-3946a3fbadf1
Set id: 469d5134-14d0-47b4-95bd-33940d4af305
Version: 1
Effective Time: 20200324
 
Newfeel