CENTECASSOL S.O.S SANITIZER- alcohol gel

CENTECASSOL S.O.S SANITIZER by

Drug Labeling and Warnings

CENTECASSOL S.O.S SANITIZER by is a Otc medication manufactured, distributed, or labeled by HANSOLBIO CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 (200ml)

INGREDIENTS AND APPEARANCE

CENTECASSOL S.O.S SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73800-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	120 g  in 200 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
TROLAMINE (UNII: 9O3K93S3TK)
TEA TREE OIL (UNII: VIF565UC2G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73800-101-02	1 in 1 BOX	03/25/2020
1	NDC: 73800-101-01	200 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/25/2020

Labeler - HANSOLBIO CO., LTD (694046931)

Registrant - HANSOLBIO CO., LTD (694046931)

Establishment
Name	Address	ID/FEI	Business Operations
HANSOLBIO CO., LTD		694046931	manufacture(73800-101)