PURELL ADVANCED INSTANT HAND SANITISER ALOE GEL- alcohol gel

PURELL Advanced Instant Hand Sanitiser Aloe Gel by

Drug Labeling and Warnings

PURELL Advanced Instant Hand Sanitiser Aloe Gel by is a Otc medication manufactured, distributed, or labeled by GOJO Industries, Inc., KDC/ONE Development Corporation, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURELL ADVANCED INSTANT HAND SANITISER ALOE GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-733
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-733-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2013
2	NDC: 21749-733-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2013
3	NDC: 21749-733-10	295 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2013
4	NDC: 21749-733-20	591 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2013
5	NDC: 21749-733-33	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
export only		05/30/2013

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		036424534	MANUFACTURE(21749-733)