PURELL ADVANCED HAND SANITIZER NOURISHING- alcohol gel
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 Nourishing

Active ingredient

Ethyl Alcohol 70%

Purpose

Antimicrobial

Use

Hand sanitizer to help decrease bacteria on 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

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

Other Information

• Store below 110°F (43°C) • May discolor certain fabrics or surfaces

Inactive Ingredients

Water (Aqua), Isopropyl Alcohol, Glycerin, Caprylyl Glycol, Isopropyl Myristate, Linum Usitatissimum (Linseed) Seed Extract, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum)

Product Label

PURELL ADVANCED HAND SANITIZER NOURISHING
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21749-485
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:21749-485-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/30/2016
2	NDC:21749-485-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/30/2016
3	NDC:21749-485-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/30/2016
4	NDC:21749-485-12	354 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/30/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	12/30/2016

Labeler - GOJO Industries, Inc. (004162038)

Name	Address	ID/FEI	Business Operations
Establishment
GOJO Industries, Inc.		036424534	manufacture(21749-485)