CENTECASSOL S.O.S SANITIZER- alcohol gel 
HANSOLBIO 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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CENTECASSOL S.O.S SANITIZER

Active ingredient

Alcohol (60%)

Purpose

Antibacterial

Uses

Uses Hand sanitizer for decreasing bacteria on skin

Warnings

For external use only

Do not use if you are allergic to any of the ingredients

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. avoid contact with broken, irritated, or itching skin. Do not puncture or incinerate.

Stop use and ask a doctor ifirritation or redness develops and condition persists for more than 72 hours

If pregnant or breast-feeding, ask a health professional before use.

Directions

Take appropriate amount onto your hand and spread it all the way to fingertips. Rub the contents until it dries

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Inactive ingredients

Water, Centella Asiatica Extract, Carbomer, Triethanolamine, Melaleuca Alternifolia (Tea Tree) Leaf Oil

CENTECASSOL S.O.S SANITIZER (60ml)

centecassol sos saniti

CENTECASSOL S.O.S SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73800-100
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL36 g  in 60 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)  
TROLAMINE (UNII: 9O3K93S3TK)  
TEA TREE OIL (UNII: VIF565UC2G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73800-100-021 in 1 BOX03/25/2020
1NDC:73800-100-0160 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/25/2020
Labeler - HANSOLBIO CO., LTD (694046931)
Registrant - HANSOLBIO CO., LTD (694046931)
Establishment
NameAddressID/FEIBusiness Operations
HANSOLBIO CO., LTD694046931manufacture(73800-100)

Revised: 3/2020
Document Id: a1ab45b8-b242-d351-e053-2a95a90a03ac
Set id: a1ab45b8-b241-d351-e053-2a95a90a03ac
Version: 1
Effective Time: 20200325
 
HANSOLBIO CO., LTD