PURELL ADVANCED HAND SANITIZER NATURALS GEL- alcohol gel 
GOJO Industries, Inc.

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PURELL Advanced Hand Sanitizer Naturals Gel

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin

Warnings

Flammable. Keep away from fire or flame. 

For external use only

When using this productdo not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor ifirritation 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

Inactive Ingredients:

Water (Aqua), Isopropyl Alcohol, Caprylyl glycol, Citrus Aurantium Dulcis (Orange) Peel Oil, Glycerin, Isopropyl Myristate, Lavandula Hybrida (Lavandin) oil, Litsea Cubeba Fruit Oil, Pelargonium Graevolens (Geranium) oil, Pogostemon Cablin Oil, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol

Product Label

PURELL ADVANCED HAND SANITIZER NATURALS GEL 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-625
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
BITTER ORANGE OIL (UNII: 9TLV70SV6I)  
LAVANDIN OIL (UNII: 9RES347CKG)  
LITSEA OIL (UNII: 2XIW34BN6O)  
GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
PATCHOULI OIL (UNII: F3IN55X5PO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:21749-625-0130 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/2016
2NDC:21749-625-0259 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/2016
3NDC:21749-625-04118 mL in 1 PACKAGE; Type 0: Not a Combination Product12/15/201912/31/2023
4NDC:21749-625-08236 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/2016
5NDC:21749-625-29295 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/2016
6NDC:21749-625-12355 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/2016
7NDC:21749-625-28828 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/2016
8NDC:21749-625-101000 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/201610/31/2023
9NDC:21749-625-24710 mL in 1 PACKAGE; Type 0: Not a Combination Product08/01/2021
10NDC:21749-625-65192 mL in 1 PACKAGE; Type 0: Not a Combination Product07/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)01/01/2016
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.036424534manufacture(21749-625)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.088312414manufacture(21749-625) , label(21749-625) , pack(21749-625)

Revised: 12/2024
Document Id: 28ec3da7-59d4-3fef-e063-6394a90ada7c
Set id: b36013d2-96a6-4c40-ad05-8d9c0d9cdb1f
Version: 6
Effective Time: 20241210
 
GOJO Industries, Inc.