LAFLARE SANTIX HAND SANITIZER- alcohol gel

Laflare SANTIX HAND SANITIZER by

Drug Labeling and Warnings

Laflare SANTIX HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Soky C&T CO.LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: ALCOHOL70% v/v

INACTIVE INGREDIENT

Inactive ingredients:

Water, Carbomer, Aminomethyl Propanol, PEG-60 Hydrogenated Castor Oil, Sodium Hyaluronate, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Citrus Limon (Lemon) Peel Oil, Tocopheryl Acetate

PURPOSE

PURPOSE: ANTISEPTIC

WARNINGS

Warnings:

For external use only. Flammable. Keep away from heat or flame
--------------------------------------------------------------------------------------------------------
Do not use
■ in children less than 2 months of age
■ on open skin wounds
--------------------------------------------------------------------------------------------------------
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
--------------------------------------------------------------------------------------------------------
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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 help reduce bacteria on the skin
■ recommended for repeated use.

Directions

Directions

■ put enough amount onto palm and thoroughly rub until it dries.
■ children under 6 years of age should be supervised when using prosuct.

Other Information

Other Information

■ Store between 15-30C (59-86F)
■ Avoid freezing and excessive heat above 40C (104F)

Package Label : Laflare SANTIX HAND SANITIZER 500mL

Package Label : Laflare SANTIX HAND SANITIZER 1000mL

INGREDIENTS AND APPEARANCE

LAFLARE SANTIX HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76970-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	Alcohol	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AminomethylPropanol (UNII: LU49E6626Q)
PEG-60 Hydrogenated Castor Oil (UNII: 02NG325BQG)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
LEMON OIL (UNII: I9GRO824LL)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76970-010-01	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/01/2020
2	NDC: 76970-010-02	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/01/2020

Labeler - Soky C&T CO.LTD (689027803)

Registrant - Soky C&T CO.LTD (689027803)

Establishment
Name	Address	ID/FEI	Business Operations
Soky C&T CO.LTD		689027803	manufacture(76970-010)