ZOEY NATURALS ISLAND HIBISCUS HAND SANITIZER- ethyl alcohol spray

ZOEY naturals Island Hibiscus HAND SANITIZER by

Drug Labeling and Warnings

ZOEY naturals Island Hibiscus HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Absolutely Natural, Inc., Absolutely Natural. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active Ingredient

Ethyl Alcohol 70%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses  Helps reduce bacteria on the skin.

WARNINGS

Warnings

For external use only.

Flammable. Keep away from fire and flames.

When using this product Do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if: Irritation and redness develop.

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

DOSAGE & ADMINISTRATION

Directions  Spray hands thoroughly with product and allow to dry without wiping.

INACTIVE INGREDIENT

Other Ingredients  Water, fragrance.

QUESTIONS

Questions? Call us! 800-848-8498

SPL UNCLASSIFIED SECTION

DEEPLY CLEANSES, PARABEN FREE, PRESERVATIVE FREE,

ZOEY naturals™ ISLAND HIBISCUS HAND SANITIZER is made without harsh chemicals and deeply cleanses without the use of water.

Effectively kills 99.9% of germs and bacteria.

www.Zoey-Naturals.com

Manufactured by:

Absolutely Natural, Inc.

640 Atlantis Road,

Melbourne, FL 32904

Packaging

INGREDIENTS AND APPEARANCE

ZOEY NATURALS ISLAND HIBISCUS HAND SANITIZER 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70793-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	yellow (Slightly Yellow)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70793-008-04	118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/09/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/09/2020

Labeler - Absolutely Natural, Inc. (166425202)

Establishment
Name	Address	ID/FEI	Business Operations
Absolutely Natural		166425202	manufacture(70793-008)