NENA HAND SANITIZER- ethyl alcohol liquid
Ironwood Clay Company, Inc.

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.

----------

NENA Hand Sanitizer

Drug Facts

Active Ingredient

Ethyl Alcohol 72%

Purpose

Antiseptic

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

Do not use
• In children less than 2 years old. • 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 consult a health care practitioner if irritation develops.

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 when they use this product to avoid swallowing.

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

Inactive ingredients Sea Silt Extract (Water, Mineral)*, Glycerin, Aloe
Barbadensis Leaf Juice**, Vaccinium Angustifolium (Blueberry) Fruit Extract**,
Calendula Officinalis Flower Extract**, Lavandula Angustifolia (Lavender)
Essential Oil, Litsea Cubeba Fruit Oil, Polyacrylate Crosspolymer-6.

Principal Display Package

HAND SANITIZER
DÉSINFECTANT POUR MAINS

KILLS HARMFUL GERMS
AND BACTERIA

with Organic Aloe & Calendula
2 fl. oz. (60 ml) V

NENA ®

Natural Hydrating
Hand Sanitizer

*Glacial Oceanic Mineral Water **Certified Organic Ingredients

Manufactured by

IRONWOOD CLAY COMPANY INC.
RICHMOND, BC V6V 2L9 CANADA
MADE IN CANADA
NENASKINCARE.COM

6 20048 34604 7

image description

res

NENA HAND SANITIZER
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:52311-656
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
LOWBUSH BLUEBERRY (UNII: G90PX41VP0)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:52311-656-01	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/22/2020	05/05/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	04/22/2020	05/05/2024

Labeler - Ironwood Clay Company, Inc. (248997694)

Registrant - Ironwood Clay Company, Inc. (248997694)

Revised: 5/2023

Document Id: fc742d10-f881-7eda-e053-6294a90adbb3

Set id: d97bdc17-e658-401c-9530-82f2e3c80bee

Version: 4

Effective Time: 20230524

Ironwood Clay Company, Inc.