INSTANT HAND SANITIZER gel

INSTANT HAND SANITIZER by

Drug Labeling and Warnings

INSTANT HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Guangzhou Joy Claire Biological Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGERDIENT

Ethyl Alcohol 75%

PURPOSE

Antiseptic

USES

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNINGS

For external use only. Flammable. Keep away from heat or flame.

DO NOT USE

in children less than 2 months of age
on ooen skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

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 Poison Control Center right away.

DIRECTIONS

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swalloing.

Other information

Store between 15-30C (59-86F)
Avoid freezing and exessive heat aboce 40C (104F)

INACTIVE INGERDIENTS

Aloe Barbadensis Leaf Extract,Camellia Sinensis Leaf Oil.

Rosmarinus Officinalis(Rosemary) Leaf Oil, Aqua,Tea-carbomer, Parfum

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

INSTANT HAND SANITIZER 
instant hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74743-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
TEA LEAF OIL (UNII: VC855RRT77)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ROSEMARY OIL (UNII: 8LGU7VM393)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74743-009-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2020
2	NDC: 74743-009-02	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2020
3	NDC: 74743-009-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2020
4	NDC: 74743-009-04	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2020
5	NDC: 74743-009-05	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2020
6	NDC: 74743-009-06	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/17/2020

Labeler - Guangzhou Joy Claire Biological Technology Co., Ltd (418209894)

Registrant - Guangzhou Joy Claire Biological Technology Co., Ltd (418209894)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Joy Claire Biological Technology Co., Ltd		418209894	manufacture(74743-009)