NDC | 21749-705-01, 21749-705-02, 21749-705-04, 21749-705-08, 21749-705-10, 21749-705-12, 21749-705-20, 21749-705-33, 21749-705-50, 21749-705-80, 21749-705-89 |
Set ID | 3330c320-49f3-4dd0-a1bd-39c1f9632370 |
Category | HUMAN OTC DRUG LABEL |
Packager | GOJO Industries, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333E |
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
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Inactive ingredients
Water (Aqua), Isopropyl Alcohol, Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum), Blue 1 (CI 42090), Yellow 5 (CI 19140)
Distributed by: GOJO Industries, Inc. Akron, OH 44309
Questions? Tel: 1-888-4-PURELL ■ www.PURELL.com
©2011, GOJO Industries, Inc.
All rights reserved. Made in U.S.A. - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PURELL ADVANCED REFRESHING ALOE
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-705 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) ALOE VERA LEAF (UNII: ZY81Z83H0X) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-705-50 15 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/14/2012 01/01/2022 2 NDC:21749-705-01 30 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/14/2012 01/01/2022 3 NDC:21749-705-02 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/14/2012 01/01/2022 4 NDC:21749-705-04 118 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/14/2012 01/01/2022 5 NDC:21749-705-08 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/14/2012 01/01/2022 6 NDC:21749-705-10 295 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/14/2012 01/01/2022 7 NDC:21749-705-12 354 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/14/2012 01/01/2022 8 NDC:21749-705-20 591 mL in 1 PACKAGE; Type 1: Convenience Kit of Co-Package 03/14/2012 01/01/2022 9 NDC:21749-705-80 800 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/14/2012 01/01/2022 10 NDC:21749-705-33 1000 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/14/2012 01/01/2022 11 NDC:21749-705-89 1200 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/14/2012 01/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/14/2012 01/01/2022 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 MANUFACTURE(21749-705) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 088312414 MANUFACTURE(21749-705) , label(21749-705) , pack(21749-705)