NENA ANTIBACTERIAL HAND SANITIZER- ethyl alcohol gel

NENA Antibacterial Hand Sanitizer by

Drug Labeling and Warnings

NENA Antibacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ironwood Clay Company, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active Ingredient

Ethyl Alcohol 73%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses
Kills harmful bacteria and germs. For personal hand hygiene to help prevent
the spread of bacteria. For use when soap and water are not available.

WARNINGS

Warnings
For external use only. Flammability.
Keep away from open flame and sources of heat.

DO NOT USE

Do not use
In children less than 2 years old.
On open skin wounds.

WHEN USING

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

STOP USE

Stop use and consult a health care practitioner if irritation develops.

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.

DOSAGE & ADMINISTRATION

Directions
Place enough product on hands to cover all surfaces.
Rub hands together until dry.
Supervise children when they use this product to avoid swallowing.

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT

Inactive ingredients aqua, glycerin, lavandula angustifolia (lavender)
essential oil, litsea cubeba fruit oil, polyacrylate crosspolymer-6.

Product Label

ANTIBACTERIAL
HAND SANITIZER

KILLS HARMFUL GERMS
AND BACTERIA

with Lavender & Litsea
4 fl. oz. (118 ml) NDC: 52311-675-01

NENA®

ANTIBACTERIAL HAND SANITIZER GEL

Sulfate & Paraben Free
Gluten Free Vegan Friendly

Manufactured by
IRONWOOD CLAY COMPANY INC.
RICHMOND, BC V6V 2L9 CANADA
MADE IN CANADA

NENASKINCARE.COM

6 20048 34605 4

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INGREDIENTS AND APPEARANCE

NENA ANTIBACTERIAL HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52311-675
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	73 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
LAVENDER OIL (UNII: ZBP1YXW0H8)
LITSEA OIL (UNII: 2XIW34BN6O)
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52311-675-01	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/14/2020

Labeler - Ironwood Clay Company, Inc. (248997694)

Registrant - Ironwood Clay Company, Inc. (248997694)