NDC | 21749-700-00, 21749-700-01, 21749-700-02, 21749-700-03, 21749-700-04, 21749-700-07, 21749-700-08, 21749-700-10, 21749-700-12, 21749-700-15, 21749-700-20, 21749-700-29, 21749-700-45, 21749-700-47, 21749-700-59, 21749-700-60, 21749-700-67, 21749-700-80, 21749-700-89 |
Set ID | 49bce138-8be2-4bf4-9eeb-f354308cd594 |
Category | HUMAN OTC DRUG LABEL |
Packager | GOJO Industries, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333E |
- Active ingredient
- Purpose
- Use
- Warnings
- Directions
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PURELL ADVANCED INSTANT HAND SANITIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-700 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:21749-700-02 24 in 1 CASE 05/10/2011 1 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:21749-700-10 8 in 1 CASE 05/10/2011 2 1000 mL in 1 BAG; Type 0: Not a Combination Product 3 NDC:21749-700-89 4 in 1 CASE 05/10/2011 3 1200 mL in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:21749-700-20 4 in 1 CASE 05/10/2011 4 2000 mL in 1 BAG; Type 0: Not a Combination Product 5 NDC:21749-700-67 4 in 1 CASE 05/10/2011 5 2000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 6 NDC:21749-700-04 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 7 NDC:21749-700-80 800 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 8 NDC:21749-700-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 9 NDC:21749-700-07 222 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 10 NDC:21749-700-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 11 NDC:21749-700-59 590 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 12 NDC:21749-700-15 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 13 NDC:21749-700-60 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 14 NDC:21749-700-47 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 15 NDC:21749-700-03 89 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 16 NDC:21749-700-08 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 17 NDC:21749-700-00 1.2 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2016 18 NDC:21749-700-45 450 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2016 19 NDC:21749-700-29 295 mL in 1 PACKAGE; Type 0: Not a Combination Product 09/28/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/10/2011 Labeler - GOJO Industries, Inc. (004162038) Registrant - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-700) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 088312414 manufacture(21749-700) , label(21749-700) , pack(21749-700) Establishment Name Address ID/FEI Business Operations Travis Association for the Blind 026032268 pack(21749-700)