Purell Advanced Refreshing Aloe

Dosage form: gel
Ingredients: ALCOHOL 0.7mL in 1mL
Labeler: GOJO Industries, Inc.
NDC code: 21749-705

Medically reviewed by Drugs.com. Last updated on Dec 23, 2024.

PURELL Advanced Hand Sanitizer Refreshing Aloe

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

Put enough product in your palm to cover hands and rub hands together briskly until dry
Children under 6 years of age should be supervised when using PURELL

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum), Blue 1 (CI 42090), Yellow 5 (CI 19140)

Distributed by: GOJO Industries, Inc. Akron, OH 44309
Questions? Tel: 1-888-4-PURELL ￭ www.PURELL.com
©2011, GOJO Industries, Inc.
All rights reserved. Made in U.S.A.

PURELL ADVANCED REFRESHING ALOE
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21749-705
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (ALCOHOL)	ALCOHOL	0.7 mL in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER
ISOPROPYL ALCOHOL
ALOE VERA LEAF
CAPRYLYL GLYCOL
GLYCERIN
ISOPROPYL MYRISTATE
.ALPHA.-TOCOPHEROL ACETATE, D-
AMINOMETHYLPROPANOL
FD&C BLUE NO. 1
FD&C YELLOW NO. 5

Packaging
#	Item Code	Package Description
1	NDC:21749-705-50	15 mL in 1 PACKAGE
2	NDC:21749-705-01	30 mL in 1 PACKAGE
3	NDC:21749-705-02	59 mL in 1 BOTTLE
4	NDC:21749-705-04	118 mL in 1 PACKAGE
5	NDC:21749-705-08	236 mL in 1 BOTTLE
6	NDC:21749-705-10	295 mL in 1 PACKAGE
7	NDC:21749-705-12	354 mL in 1 BOTTLE
8	NDC:21749-705-20	591 mL in 1 PACKAGE
9	NDC:21749-705-80	800 mL in 1 PACKAGE
10	NDC:21749-705-33	1000 mL in 1 PACKAGE
11	NDC:21749-705-89	1200 mL in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/14/2012	01/01/2022

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Operations
GOJO Industries, Inc.		036424534	MANUFACTURE(21749-705)

Establishment
Name	Address	ID/FEI	Operations
GOJO Industries, Inc.		088312414	MANUFACTURE(21749-705), label(21749-705), pack(21749-705)

Revised: 01/2022

Document Id: 673d90bd-dab5-45ba-ae59-127e583a0edb

Set id: 3330c320-49f3-4dd0-a1bd-39c1f9632370

Version: 4

Effective Time: 20220101

GOJO Industries, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer

Purell Advanced Refreshing Aloe

Further information

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