PURELL ADVANCED WITH ALOE INSTANT HAND SANITIZER- 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 with Aloe Instant Hand Sanitizer

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Use

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

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
Children under 6 years of age should be supervised when using this product.

Inactive ingredients

Water (Aqua), Isoproyl Alcohol, Aloe Barbadensis Lead 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)

Product Label

PURELL ADVANCED WITH ALOE INSTANT HAND SANITIZER
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21749-703
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.70 mL in 1 mL

Ingredient Name	Strength
Inactive Ingredients
Water (UNII: 059QF0KO0R)
Isopropyl Alcohol (UNII: ND2M416302)
Glycerin (UNII: PDC6A3C0OX)
Isopropyl Myristate (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
Caprylyl Glycol (UNII: 00YIU5438U)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
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:21749-703-10	1000 mL in 1 PACKAGE; Type 0: Not a Combination Product	05/05/2011	01/01/2022
2	NDC:21749-703-20	2000 mL in 1 PACKAGE; Type 0: Not a Combination Product	05/05/2011	01/01/2022
3	NDC:21749-703-89	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/05/2011	01/01/2022
4	NDC:21749-703-12	354 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/05/2011	01/01/2022
5	NDC:21749-703-80	800 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/05/2011	01/01/2022
6	NDC:21749-703-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/05/2011	01/01/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	05/05/2011	01/01/2022

Labeler - GOJO Industries, Inc. (004162038)

Name	Address	ID/FEI	Business Operations
Establishment
GOJO Industries, Inc.		036424534	manufacture(21749-703)

Name	Address	ID/FEI	Business Operations
Establishment
GOJO Industries, Inc.		088312414	manufacture(21749-703) , label(21749-703) , pack(21749-703)

Revised: 1/2022

Document Id: d06a5133-2638-4c5f-806e-5d776d7fc4e1

Set id: 8ffe7751-4bee-482c-ac50-ae4d6156657b

Version: 4

Effective Time: 20220101

GOJO Industries, Inc.