DEOPROCE ALL CLEAN HAND SANITIZER by HANDY LABS / Greencos Co., Ltd.

DEOPROCE ALL CLEAN HAND SANITIZER by

Drug Labeling and Warnings

DEOPROCE ALL CLEAN HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by HANDY LABS, Greencos Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DEOPROCE ALL CLEAN HAND SANITIZER- ethyl alcohol gel 
HANDY LABS

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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ACTIVE INGREDIENT

ETHYL ALCOHOL 62%

INACTIVE INGREDIENTS

WATER, PROPYLENE GLYCOL, HYDROXYPROPYL METHYLCELLULOSE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, TRIETHANOLAMINE, GLYCERIN, FRAGRANCE, SODIUM CHLORIDE, BUTYLENE GLYCOL, DIPROPYLENE GLYCOL, 1,2-HEXANEDIOL, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, LIMONENE

PURPOSE

ANTISEPTIC

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

Hand sanitizer to help reduce bacteria that potentially can cause disease.

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 swallowing.

Other information

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DEOPROCE ALL CLEAN HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79296-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	310 mL  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	Â
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	Â
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)	Â
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)	Â
TROLAMINE (UNII: 9O3K93S3TK)	Â
GLYCERIN (UNII: PDC6A3C0OX)	Â
SODIUM CHLORIDE (UNII: 451W47IQ8X)	Â
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	Â
DIPROPYLENE GLYCOL (UNII: E107L85C40)	Â
1,2-HEXANEDIOL (UNII: TR046Y3K1G)	Â
ROSEMARY (UNII: IJ67X351P9)	Â
GREEN TEA LEAF (UNII: W2ZU1RY8B0)	Â
LIMONENE, (+)- (UNII: GFD7C86Q1W)	Â

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79296-010-01	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2020	03/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/01/2020	03/01/2021

Labeler - HANDY LABS (695520626)

Registrant - HANDY LABS (695520626)

Establishment
Name	Address	ID/FEI	Business Operations
GreenCos Co., Ltd.		694777325	manufacture(79296-010)

Revised: 5/2021

Document Id: e8ad7cc6-8d47-4feb-96ba-fdf8893965e8

34390-5

Set id: 73676704-3743-43ac-9223-e93500d9aba2

Version: 2

Effective Time: 20210525

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