PURELL ADVANCED HAND SANITIZER NATURALS FOAM- alcohol liquid
GOJO Industries, 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.

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PURELL Advanced Hand Sanitizer Naturals Foam

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Uses

Hand sanitizer to help reduce bacteria on the skin

Warnings

Flammable. Keep away from fire or flame.

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts

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

Directions

Place enough product in your palm to thoroughly cover your hands
Run hands together briskly until dry
Children under 6 years of age should be supervised when using this product

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, PEG-12 Dimethicone, Caprylyl Glycol, Citrus Aurantium Dulcis (Orange) Peel Oil, Glycerin, Lavandula Hybrida (Lavandin) Oil, Litsea Cubeba Fruit Oil, Pelargonium Graveolens (Geranium) Oil, Pogostemon Cablin Oil

Product Label

PURELL ADVANCED HAND SANITIZER NATURALS FOAM
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21749-875
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ORANGE OIL, COLD PRESSED (UNII: AKN3KSD11B)
GLYCERIN (UNII: PDC6A3C0OX)
LAVANDIN OIL (UNII: 9RES347CKG)
LITSEA OIL (UNII: 2XIW34BN6O)
PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
POGOSTEMON CABLIN LEAF OIL (UNII: F3IN55X5PO)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:21749-875-10	295 mL in 1 PACKAGE; Type 0: Not a Combination Product	04/15/2021
2	NDC:21749-875-50	500 mL in 1 PACKAGE; Type 0: Not a Combination Product	04/15/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	04/15/2021

Labeler - GOJO Industries, Inc. (004162038)

Name	Address	ID/FEI	Business Operations
Establishment
GOJO Industries, Inc.		036424534	manufacture(21749-875) , pack(21749-875) , label(21749-875)