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 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 shodl be supervised when using this product

Other information

• Store below 110°F (43°C)

• May discolor certain fabrics or surfaces

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, 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 HAND SANITIZER BE VIBRANT
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21749-028
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)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:21749-028-01	30 mL in 1 PACKAGE; Type 0: Not a Combination Product	12/22/2016
2	NDC:21749-028-02	59 mL in 1 PACKAGE; Type 0: Not a Combination Product	12/22/2016
3	NDC:21749-028-04	118 mL in 1 PACKAGE; Type 0: Not a Combination Product	12/22/2016
4	NDC:21749-028-08	236 mL in 1 PACKAGE; Type 0: Not a Combination Product	12/22/2016
5	NDC:21749-028-10	295 mL in 1 PACKAGE; Type 0: Not a Combination Product	12/22/2016
6	NDC:21749-028-12	354 mL in 1 PACKAGE; Type 0: Not a Combination Product	12/22/2016
7	NDC:21749-028-45	450 mL in 1 PACKAGE; Type 0: Not a Combination Product	12/22/2016
8	NDC:21749-028-16	473 mL in 1 PACKAGE; Type 0: Not a Combination Product	12/22/2016
9	NDC:21749-028-20	591 mL in 1 PACKAGE; Type 0: Not a Combination Product	12/22/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	12/22/2016

Labeler - GOJO Industries, Inc. (004162038)

Name	Address	ID/FEI	Business Operations
Establishment
GOJO Industries, Inc.		036424534	manufacture(21749-028)