![PURELL ADVANCED HAND SANITIZER GEL (ALCOHOL) GEL [GOJO INDUSTRIES, INC.]](https://medic.hrt.org//dailymed/images/f9a3c157-3a6f-4fcc-adcc-0a11f643e836/label 2.jpg)
![PURELL ADVANCED HAND SANITIZER GEL (ALCOHOL) GEL [GOJO INDUSTRIES, INC.]](https://medic.hrt.org//dailymed/images/f9a3c157-3a6f-4fcc-adcc-0a11f643e836/label.jpg)
| NDC | 21749-032-01, 21749-032-02, 21749-032-05, 21749-032-10, 21749-032-12, 21749-032-45, 21749-032-53, 21749-032-89, 21749-032-97 |
| Set ID | f9a3c157-3a6f-4fcc-adcc-0a11f643e836 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | GOJO Industries, Inc. |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number |
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
PURELL ADVANCED HAND SANITIZER GEL
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-032 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) 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-032-01 60 mL in 1 PACKAGE; Type 0: Not a Combination Product 12/01/2014 2 NDC:21749-032-45 450 mL in 1 PACKAGE; Type 0: Not a Combination Product 12/01/2014 3 NDC:21749-032-53 535 mL in 1 PACKAGE; Type 0: Not a Combination Product 12/01/2014 4 NDC:21749-032-97 700 mL in 1 PACKAGE; Type 0: Not a Combination Product 12/01/2014 5 NDC:21749-032-10 1000 mL in 1 PACKAGE; Type 0: Not a Combination Product 12/01/2014 6 NDC:21749-032-89 1200 mL in 1 PACKAGE; Type 0: Not a Combination Product 12/01/2014 7 NDC:21749-032-02 30 mL in 1 PACKAGE; Type 0: Not a Combination Product 12/01/2015 8 NDC:21749-032-12 354 mL in 1 PACKAGE; Type 0: Not a Combination Product 12/01/2015 9 NDC:21749-032-05 1.2 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date export only 12/01/2014 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-032)
