HANDS PURI PLUS HAND SANITIZING MIST- alcohol spray

Hands Puri Plus Hand Sanitizing Mist by

Drug Labeling and Warnings

Hands Puri Plus Hand Sanitizing Mist by is a Otc medication manufactured, distributed, or labeled by Honest Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: ALCOHOL 70% v/v

INACTIVE INGREDIENT

Inactive ingredients:

Water, Glycerin, Butylene Glycol, 1,2-Hexanediol, Aloe Barbadensis Leaf Extract

PURPOSE

Purpose: ANTISEPTIC

WARNINGS

Warnings:

For external use only. Flammable. Keep away from heat or flame
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Do not use
in children less than 2 months of age
on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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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 sanitizing mist to help reduce bacteria that potentially can cause disease.

Directions

Directions:

Spray enough product on hands to cover all surfaces. Rub hands together until dry.
Spray on hands, clothes and belongings and allow to dry.
Children under 6 years of age should be supervised when using the product

Other information

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HANDS PURI PLUS HAND SANITIZING MIST 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76904-080
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	350 mL  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Butylene Glycol (UNII: 3XUS85K0RA)
1,2-Hexanediol (UNII: TR046Y3K1G)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76904-080-01	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2020

Labeler - Honest Co., Ltd. (694773213)

Registrant - Honest Co., Ltd. (694773213)

Establishment
Name	Address	ID/FEI	Business Operations
Honest Co., Ltd.		694773213	manufacture(76904-080)