GREEN EKII HAND SANITIZER- alcohol gel

green ekii hand sanitizer by

Drug Labeling and Warnings

green ekii hand sanitizer by is a Otc medication manufactured, distributed, or labeled by laboratorios funat sas. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

OTC - ACTIVE INGREDIENT SECTION

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl alcohol 60% v/v

OTC - PURPOSE SECTION

OTC - PURPOSE SECTION

Purpose

atimicrobial

INDICATIONS & USAGE SECTION

INDICATIONS & USAGE SECTION

Use

Hand sanitizer to help reduce bacteria on the skin

Recommended for repeated use

WARNINGS SECTION

WARNINGS SECTION

Warnings

Flammable. keep away from fire or flame

For external use only

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

stop use and ask doctor if irritation or rash appears and lasts

keep out of reach of children . if swallowed, get medical help or contact a poison control center right away

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

DOSAGE & ADMINISTRATION SECTION

Directions

Put enough product into palms, spread on both hands and rub hands vigorously until dry

children under 6 years should be supervised when using this product

OTHER SAFETY INFORMATION

OTHER SAFETY INFORMATION

Other information

store below 110ºF (43ºc)

May discolor certain fabrics

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water (Aqua),

Aloe Barbadensis leaf juice

acrylates/C10-30 alkyl acrylate crosspolymer

glycerin

triethanolamine

fragrance (parfum).

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

green ekii

hand sanitizer

kills 99.99% of germs

with aloe vera extract to soften and moisturize hands

7.76 oz (220 gr)

INGREDIENTS AND APPEARANCE

GREEN EKII HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73781-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)	1.15 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX)	0.5 g  in 100 g
TROLAMINE (UNII: 9O3K93S3TK)	0.9 g  in 100 g
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)	0.8 g  in 100 g
WATER (UNII: 059QF0KO0R)	36.55 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73781-001-01	220 g in 1 BOTTLE, PLASTIC; 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 - laboratorios funat sas (881335918)