Back Label NDC 79206-002-02

Back Label NDC 79206-001-05

Active ingredient[s] Purpose

Isopropyl alcohol 70%v/v…….………….……………..................Antiseptic

Use[s]

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 open skin wounds

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

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. If swallowed, get medical help, or contact a 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 swallowing.

Other information

• Store between 15-30C (59-86F)

• Avoid freezing and excessive heat above 40C (104F)

NDC 79206-001

Inactive ingredients

Glycerin, Carbomer, Triisopropanolamine, Aloe Vera Juice, Iodopropynyl Butylcarbamate, Diazolidinyl Urea, hydrogen peroxide, fragrance, purified water USP

NDC 79206-002

Inactive ingredients

Glycerin, Carbomer, Triisopropanolamine, Aloe Vera Juice, Iodopropynyl Butylcarbamate, Diazolidinyl Urea, hydrogen peroxide, purified water USP

Manufacture and Distribution
Made in the USA by
F & E Group LLP
Kalamazoo, MI. 49004.
Email: info@the-essenceofvea.com
Text: (269)-267-2015
www.the-essenceofeva.com
Batch No. 001 Mfg.: June /2020.
Best Used within 1 year of Manufacture

Company details

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.

Primary label front NDC 79206-002-02
236 mL

Front label NDC 79206-002-02

Primary Label Front NDC 79206-001-05
236 mL

Primary Label Front NDC 79206-001-05

THE ESSENCE OF EVA
hand sanitizer with aloe gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:79206-002
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
GLYCERIN (UNII: PDC6A3C0OX)	2 mL in 100 mL
WATER (UNII: 059QF0KO0R)	15 mL in 100 mL
ALOE (UNII: V5VD430YW9)	35 mL in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.125 mL in 100 mL

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:79206-002-02	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/19/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	06/19/2020

THE ESSENCE OF EVA
summer citrus hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:79206-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
LIME (CITRUS) (UNII: 8CZS546954)	0.2 mL in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.125 mL in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	2 mL in 100 mL
WATER (UNII: 059QF0KO0R)	15 mL in 100 mL
ALOE (UNII: V5VD430YW9)	35 mL in 100 mL

Product Characteristics
Color		Score
Shape		Size
Flavor	CITRUS (A sunny, seaside blend of fresh Key lime, Italian bergamot, French lavender, crushed herbs, beach juniper and warm sands.)	Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:79206-001-05	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/19/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	06/19/2020

Labeler - F & E Group LLP (117556801)