Active Ingredients:

Organic Ethanol 62%

Purpose:

Antiseptic

Uses:

For hand washing to decrease bacteria on skin
Recommended for repeated use

Warnings:

Flammable, keep away from fire/flame
For external use only
Do not use in eyes. If contact occurs, flush thoroughly with water.
Stop use and ask a doctor if redness and irritation develop and persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact the Poison Control center right away.

Directions:

Wet hands thoroughly with product and allow to dry without wiping.
Do not use other than intended.

Other Information:

Store below 104°F (40°C).
May discolor certain fabrics.

Inactive Ingredients:

Purified Water, Organic Mentha Piperita (Peppermint) Oil, Organic Thymus Vulgaris (Thyme) Leaf Extract, Vegetable Glycerin, Tocopherol

ESSENTIAL OILS

USDA ORGANIC

HAND sanitizer SPRAY

peppermint

99.9% EFFECTIVE AGAINST MOST COMMON GERMS
made with moisturizing ingredients

SYNTHETIC FRAGRANCE FREE

TRICLOSAN FREE • BENZALKONIUM CHLORIDE FREE
MADE WITH ORGANIC INGREDIENTS • PHTHALATE FREE

EO® PRODUCTS
SMALL WORLD TRADING CO. SAN RAFAEL, CA 94901
MADE IN THE USA FROM DOMESTIC AND GLOBALLY SOURCED INGREDIENTS
800-570-3775 eoproducts.com
CERTIFIED ORGANIC BY CCOF

Packaging

image description

EO HAND SANITIZER PEPPERMINT
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54748-102
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
WATER (UNII: 059QF0KO0R)
PEPPERMINT OIL (UNII: AV092KU4JH)
THYMUS VULGARIS LEAF (UNII: GRX3499643)
GLYCERIN (UNII: PDC6A3C0OX)
TOCOPHEROL (UNII: R0ZB2556P8)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54748-102-01	10 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/15/2013
2	NDC:54748-102-12	12 in 1 BOX	08/13/2018
2	NDC:54748-102-01	10 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
3	NDC:54748-102-02	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/15/2013	11/30/2016
4	NDC:54748-102-05	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/02/2017
5	NDC:54748-102-09	6 in 1 BOX	08/13/2018
5	NDC:54748-102-05	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/15/2013

Labeler - EO Products, LLC (786611210)

Name	Address	ID/FEI	Business Operations
Establishment
EO Products, LLC		786611210	manufacture(54748-102)

Drug Facts