Active Ingredient

Alcohol 62% (v/v)

Purpose

Anti-Bacterial

Uses

■ Hand sanitizer to help reduce bacteria on the skin

Warnings

■ Flammable. Keep away from fire or flame.

When using this product

■ do not use in or near eyes. In case of contact, rinse eyes throughly with water

Stop use and ask a doctor if

■ irritation or redness develop and last for more than 72 hours

Keep out of reach of children

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

Directions

■ Dispense and rub onto hands until dry. Do not rinse off.

■ Children under 6 years of age should use this product under supervision.

■ repeat as necessary

Other information

■ Do not store above 110°F (43°C)

Inactive ingredients

Aloe Barbadensis (aloe vera) Leaf Juice, Butyrospermum Parkii (Shea) Butter, Glycerin, Lavandula Angustifolia (Lavender) Oil, Panthenol, Polyacrylate Crosspolymer-6, Water (Aqua)

GenRx Hand Sanitizing Gel with Lavender

Manufactured in the USA by PureTek Corporation
Panorama City, CA 91402 USA
877-921-7873
www.genrxwoundcare.com

List No:41431JLA

NDC 59088-413-08

4 floz Label

NDC 59088-413-31

16.9 floz

NDC 59088-413-39

24 FLOZ

HAND SANITIZING WITH LAVENDER OIL
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:59088-413
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PANTHENOL (UNII: WV9CM0O67Z)
WATER (UNII: 059QF0KO0R)
SHEA BUTTER (UNII: K49155WL9Y)
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C)
LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:59088-413-06	1 in 1 KIT	06/05/2020
1	NDC:59088-413-39	710 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC:59088-413-36	1 in 1 KIT	06/05/2020
2	NDC:59088-413-14	1 in 1 KIT
2	NDC:59088-413-08	118 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC:59088-413-31	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/05/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M014	06/05/2020

Labeler - PureTek Corporation (785961046)

Name	Address	ID/FEI	Business Operations
Establishment
PureTek Corporation		785961046	manufacture(59088-413) , label(59088-413)