BENOA PREMIUM HAND SANITIZER- alcohol gel 
Natuzen Co.,Ltd.

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ACTIVE INGREDIENT

Active ingredients: Ethyl alcohol 70%

INACTIVE INGREDIENT

Inactive ingredients:

Water, Butylene Glycol, Carbomer, Triethanolamine, PEG-60 Hydrogenated Castor Oil, Glycyrrhiza Uralensis (Licorice) Root Extract, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Fragrance, Citral, Limonene

PURPOSE

Purpose: Hand Sanitizer

WARNINGS

Warnings:

• Flammable. Keep away from fire or flame.
• For external use only.
• When using this product do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.
• Stop use and ask a doctor if irritation or rash appears and lasts.
• Keep Out of Reach of Children.
• Do not eat.
• 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

Uses

Uses:
Hand sanitizer to help reduce bacteria on the skin

Directions

Directions:
• Put 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. Not recommended for infants.

Other information

Other information
• Store below 110’F (43’C)
• May discolor certain fabrics or surfaces

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

BENOA PREMIUM HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70930-110
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL350 mL  in 500 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Butylene Glycol (UNII: 3XUS85K0RA)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
TROLAMINE (UNII: 9O3K93S3TK)  
PEG-60 Hydrogenated Castor Oil (UNII: 02NG325BQG)  
GLYCYRRHIZA URALENSIS ROOT (UNII: 42B5YD8F0K)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CITRAL (UNII: T7EU0O9VPP)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70930-110-01500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/01/202012/30/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00304/01/202012/30/2023
Labeler - Natuzen Co.,Ltd. (688201272)
Registrant - Natuzen Co.,Ltd. (688201272)
Establishment
NameAddressID/FEIBusiness Operations
Natuzen Co.,Ltd.688201272manufacture(70930-110)

Revised: 4/2024
 
Natuzen Co.,Ltd.