PURELL ADVANCED REFRESHING ALOE- 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 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.

Product Label

PURELL ADVANCED REFRESHING ALOE
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21749-705
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)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:21749-705-50	15 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/14/2012	01/01/2022
2	NDC:21749-705-01	30 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/14/2012	01/01/2022
3	NDC:21749-705-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/14/2012	01/01/2022
4	NDC:21749-705-04	118 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/14/2012	01/01/2022
5	NDC:21749-705-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/14/2012	01/01/2022
6	NDC:21749-705-10	295 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/14/2012	01/01/2022
7	NDC:21749-705-12	354 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/14/2012	01/01/2022
8	NDC:21749-705-20	591 mL in 1 PACKAGE; Type 1: Convenience Kit of Co-Package	03/14/2012	01/01/2022
9	NDC:21749-705-80	800 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/14/2012	01/01/2022
10	NDC:21749-705-33	1000 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/14/2012	01/01/2022
11	NDC:21749-705-89	1200 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/14/2012	01/01/2022

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

Labeler - GOJO Industries, Inc. (004162038)

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

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

Revised: 1/2022

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

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

Version: 4

Effective Time: 20220101

GOJO Industries, Inc.