DIIZ HAND SANITIZER- alcohol gel 
THE SUN 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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ACTIVE INGREDIENT

Active ingredients: Alcohol 70.0%

INACTIVE INGREDIENT

Inactive ingredients:

Aloe Barbadensis Leaf Extract, Citrus Paradisi (Grapefruit) Seed Extract, Disodium EDTA, Glycerin, Propylene Glycol, Carbomer, 1,2-Hexandiol, Water, Triethanolamine

PURPOSE

PURPOSE: Antimicrobial

WARNINGS

Warnings:

For external use only

Flammable. Keep away from heat and flame.

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 skin irritation or rash develops.

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

■ Hand sanitizer to 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 product.

Other Information

Other Information

■ Store below 43°C (110°F)
■ May discolor certain fabrics or surfaces

QUESTIONS

Questions

www.sacos.co.kr

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottle

DIIZ HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74923-080
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Water (UNII: 059QF0KO0R)  
CITRUS PARADISI SEED (UNII: 12F08874Y7)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
Glycerin (UNII: PDC6A3C0OX)  
Propylene Glycol (UNII: 6DC9Q167V3)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74923-080-01500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/01/2020
Labeler - THE SUN CO.LTD (694433104)
Registrant - THE SUN CO.LTD (694433104)
Establishment
NameAddressID/FEIBusiness Operations
THE SUN CO.LTD694433104manufacture(74923-080)

Revised: 5/2020
Document Id: 3650bc38-2da4-42d1-afaf-f12904dcbd80
Set id: 112e631b-7184-4420-9636-c539a5f0b715
Version: 2
Effective Time: 20200501
 
THE SUN CO.LTD