PURELL ADVANCED HAND SANITIZER ULTRA NOURISHING FOAM- alcohol liquid

PURELL Advanced Hand Sanitizer ULTRA NOURISHING Foam by

Drug Labeling and Warnings

PURELL Advanced Hand Sanitizer ULTRA NOURISHING Foam by is a Otc medication manufactured, distributed, or labeled by GOJO Industries, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Uses

 Hand sanitizer to help reduce bacteria on the skin that could cause disease

Recommended for repeated use

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

 Rub hands together briskly until dry

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, PEG-12 Dimethicone, Avena Sativa (Oat) Kernel Extract, Caprylyl glycol, Glycerin, Niaciniamide, PPG-12/SMDI copolymer, Potassium Sorbate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURELL ADVANCED HAND SANITIZER ULTRA NOURISHING FOAM 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-856
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)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
OAT (UNII: Z6J799EAJK)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERIN (UNII: PDC6A3C0OX)
NIACINAMIDE (UNII: 25X51I8RD4)
PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-856-17	515 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/04/2023
2	NDC: 21749-856-40	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/04/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/04/2023

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		036424534	manufacture(21749-856) , pack(21749-856) , label(21749-856)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		088312414	manufacture(21749-856) , pack(21749-856) , label(21749-856)