ELIVE HAND SANITIZER- alcohol gel
Provendex Pty Ltd

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.

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ELIVE Hand Sanitizer

Drug Facts

Active ingredient

Ethyl alcohol 72%

Purpose

Antiseptic

Use

for hand washing to decrease bacteria on the skin

Warnings

For external use only
Flammable, keep away from fire or flame.

Do not use

in the eyes

Stop use and ask a doctor if

irritation and redness develop
condition persists 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

wet hands thoroughly with product and allow to dry without wiping

Inactive ingredients

water, glycerin, jojoba oil PEG-150 esters, tocopherol, aloe vera extract, panthenol, Japanese honeysuckle flower extract, wild chrysanthemum flower extract, Sophora ( Sophora angustifolia) root extract, peppermint leaf extract, Chinese skullcap root extract, acylates/C10-30 alkyl acrylate crosspolymer, triethanolamine.

Package Labeling:240ml

240ml Label 240ml Label2

Package Labeling:500ml

500ml Label 500ml Label2.jpg

ELIVE HAND SANITIZER
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:79123-000
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.72 mL in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
JOJOBA OIL (UNII: 724GKU717M)
TOCOPHEROL (UNII: R0ZB2556P8)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PANTHENOL (UNII: WV9CM0O67Z)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
CHRYSANTHEMUM INDICUM FLOWER (UNII: I6OER6U04L)
MENTHA PIPERITA LEAF (UNII: A389O33LX6)
TROLAMINE (UNII: 9O3K93S3TK)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:79123-000-01	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/02/2020
2	NDC:79123-000-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/02/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	07/02/2020

Labeler - Provendex Pty Ltd (742436587)