NDC | 21749-807-22, 21749-807-23, 21749-807-31, 21749-807-33, 21749-807-51, 21749-807-53, 21749-807-89, 21749-807-97 |
Set ID | 3c3b14e1-4a9d-4ebb-b6b6-ab0173ac06e5 |
Category | HUMAN OTC DRUG LABEL |
Packager | GOJO Industries, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333E |
- Active ingredient
- Purpose
- Use
- Warnings
- Directions
- Other information
- 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:21749-807 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) PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-807-31 45 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/11/2011 2 NDC:21749-807-22 200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/11/2011 3 NDC:21749-807-23 222 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/11/2011 4 NDC:21749-807-53 535 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/11/2011 5 NDC:21749-807-51 550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/11/2011 6 NDC:21749-807-33 1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/11/2011 7 NDC:21749-807-89 1200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/11/2011 8 NDC:21749-807-97 700 mL in 1 PACKAGE; Type 0: Not a Combination Product 04/11/2011 9 NDC:21749-807-30 300 mL in 1 PACKAGE; Type 0: Not a Combination Product 08/24/2020 10 NDC:21749-807-50 189271 mL in 1 PACKAGE; Type 0: Not a Combination Product 08/24/2020 11 NDC:21749-807-80 800 mL in 1 PACKAGE; Type 0: Not a Combination Product 02/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 04/11/2011 Labeler - GOJO Industries, Inc. (004162038) Registrant - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-807) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 088312414 manufacture(21749-807) , label(21749-807) , pack(21749-807)