NDC | 21749-706-08, 21749-706-10, 21749-706-12, 21749-706-89, 21749-706-97 |
Set ID | 58adb1ba-73d8-4f6a-9296-269213e2f1e8 |
Category | HUMAN OTC DRUG LABEL |
Packager | GOJO Industries, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333E |
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
PURELL ADVANCED E3 RATED INSTANT HAND SANITIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-706 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.70 mL in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Isopropyl Alcohol (UNII: ND2M416302) Glycerin (UNII: PDC6A3C0OX) Isopropyl Myristate (UNII: 0RE8K4LNJS) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) Caprylyl Glycol (UNII: 00YIU5438U) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-706-08 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/31/2013 2 NDC:21749-706-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/31/2013 3 NDC:21749-706-97 700 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/31/2013 4 NDC:21749-706-10 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/31/2013 5 NDC:21749-706-89 1200 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/31/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/31/2013 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-706) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 088312414 manufacture(21749-706) , label(21749-706) , pack(21749-706)