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, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum)

product label

PURELL ADVANCED REFRESHING
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21749-704(NDC:21749-972)
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:21749-704-01	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2012
2	NDC:21749-704-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2012
3	NDC:21749-704-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2012
4	NDC:21749-704-12	354 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2012
5	NDC:21749-704-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2012
6	NDC:21749-704-10	295 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/15/2012
7	NDC:21749-704-20	2000 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/15/2012
8	NDC:21749-704-59	591 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/15/2012
9	NDC:21749-704-50	15 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/15/2012
10	NDC:21749-704-45	450 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/15/2012
11	NDC:21749-704-33	1000 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/15/2012
12	NDC:21749-704-13	372 mL in 1 PACKAGE; Type 0: Not a Combination Product	05/07/2020
13	NDC:21749-704-16	473 mL in 1 PACKAGE; Type 0: Not a Combination Product	04/27/2020
14	NDC:21749-704-28	828 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/15/2020
15	NDC:21749-704-65	192 mL in 1 PACKAGE; Type 0: Not a Combination Product	06/01/2021
16	NDC:21749-704-24	710 mL in 1 PACKAGE; Type 0: Not a Combination Product	08/01/2021
17	NDC:21749-704-15	1500 mL in 1 PACKAGE; Type 0: Not a Combination Product	08/01/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M505G(a)(3)	03/15/2012

Labeler - GOJO Industries, Inc. (004162038)

Name	Address	ID/FEI	Business Operations
Establishment
GOJO Industries, Inc.		036424534	MANUFACTURE(21749-704)

Name	Address	ID/FEI	Business Operations
Establishment
GOJO Industries, Inc.		088312414	MANUFACTURE(21749-704) , label(21749-704) , pack(21749-704)