NDC | 21749-704-01, 21749-704-02, 21749-704-04, 21749-704-08, 21749-704-10, 21749-704-12, 21749-704-20, 21749-704-33, 21749-704-45, 21749-704-50, 21749-704-59 |
Set ID | b1beadc4-5cf4-4e28-90cc-3f9fdc132a90 |
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
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INGREDIENTS AND APPEARANCE
PURELL ADVANCED REFRESHING
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-704 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, D- (UNII: A7E6112E4N) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-704-01 29 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2012 2 NDC:21749-704-02 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2012 3 NDC:21749-704-08 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2012 4 NDC:21749-704-12 354 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2012 5 NDC:21749-704-04 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2012 6 NDC:21749-704-10 295 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/15/2012 7 NDC:21749-704-20 2000 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/15/2012 8 NDC:21749-704-59 591 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/15/2012 9 NDC:21749-704-50 15 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/15/2012 10 NDC:21749-704-45 450 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/15/2012 11 NDC:21749-704-33 1000 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/15/2012 12 NDC:21749-704-13 372 mL in 1 PACKAGE; Type 0: Not a Combination Product 05/07/2020 13 NDC:21749-704-16 473 mL in 1 PACKAGE; Type 0: Not a Combination Product 04/27/2020 14 NDC:21749-704-28 828 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/15/2020 15 NDC:21749-704-65 192 mL in 1 PACKAGE; Type 0: Not a Combination Product 06/01/2021 16 NDC:21749-704-24 710 mL in 1 PACKAGE; Type 0: Not a Combination Product 08/01/2021 17 NDC:21749-704-15 1500 mL in 1 PACKAGE; Type 0: Not a Combination Product 08/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/15/2012 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 MANUFACTURE(21749-704) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 088312414 MANUFACTURE(21749-704) , label(21749-704) , pack(21749-704) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 117957695 relabel(21749-704) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 117959271 relabel(21749-704)