HAND SANITIZER- hand sanitizer spray spray

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Shenzhen Lynns Industrial Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

75%ethyl alcohol by volume....antimicrobial

Purpose

antimicrobial

Use

Use to help reduce bacterial on skin.

Warnings

Flammable.External use only

Do not use on open skin wounds or children under 2 months of age

When using this product avoid contact with eyes.If case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Do not use

Do not use on open skin wounds or children under 2 months of age

WHEN USING

When using this product avoid contact with eyes.If case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

STOP USE

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

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.

Directions

·wet hands thoroughly with product and allow to dry without wiping.
·For children under 6, use only under adult supervision.

Other information

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

Inactive ingredients

Package Label - Principal Display Panel

81422-009-00--Hand Sanitizer Spray 500ml

81422-009-37--Hand Sanitizer Spray 1Gallon

81422-009-50--Hand Sanitizer Spray 50ml

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
hand sanitizer spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81422-009
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
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81422-009-00	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
2	NDC: 81422-009-37	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
3	NDC: 81422-009-50	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - Shenzhen Lynns Industrial Co., Ltd. (525563756)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Lynns Industrial Co., Ltd.		525563756	manufacture(81422-009)