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 LabelProduct Label

PURELL ADVANCED WITH ALOE INSTANT HAND SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-703
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.70 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:21749-703-101000 mL in 1 PACKAGE; Type 0: Not a Combination Product05/05/201101/01/2022
2NDC:21749-703-202000 mL in 1 PACKAGE; Type 0: Not a Combination Product05/05/201101/01/2022
3NDC:21749-703-891200 mL in 1 BOTTLE; Type 0: Not a Combination Product05/05/201101/01/2022
4NDC:21749-703-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product05/05/201101/01/2022
5NDC:21749-703-80800 mL in 1 BOTTLE; Type 0: Not a Combination Product05/05/201101/01/2022
6NDC:21749-703-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product05/05/201101/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/05/201101/01/2022
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.036424534manufacture(21749-703)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.088312414manufacture(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.