Label: PURELL ADVANCED SOOTHING- alcohol gel
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NDC Code(s):
21749-713-01,
21749-713-02,
21749-713-04,
21749-713-08, view more21749-713-10, 21749-713-12, 21749-713-20, 21749-713-24, 21749-713-27, 21749-713-28, 21749-713-33, 21749-713-40, 21749-713-65, 21749-713-67
- Packager: GOJO Industries, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 11, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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 SOOTHING
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-713 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:21749-713-01 30 mL in 1 PACKAGE; Type 0: Not a Combination Product 11/01/2018 02/28/2023 2 NDC:21749-713-02 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/01/2018 3 NDC:21749-713-04 118 mL in 1 PACKAGE; Type 0: Not a Combination Product 11/01/2018 4 NDC:21749-713-08 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/01/2018 5 NDC:21749-713-10 295 mL in 1 PACKAGE; Type 0: Not a Combination Product 11/01/2018 6 NDC:21749-713-12 354 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/01/2018 7 NDC:21749-713-20 591 mL in 1 PACKAGE; Type 1: Convenience Kit of Co-Package 11/01/2018 03/31/2023 8 NDC:21749-713-27 800 mL in 1 PACKAGE; Type 0: Not a Combination Product 11/01/2018 07/31/2022 9 NDC:21749-713-28 826 mL in 1 PACKAGE; Type 0: Not a Combination Product 11/01/2018 09/30/2021 10 NDC:21749-713-33 1000 mL in 1 PACKAGE; Type 0: Not a Combination Product 11/01/2018 11 NDC:21749-713-40 1200 mL in 1 PACKAGE; Type 0: Not a Combination Product 11/01/2018 03/31/2023 12 NDC:21749-713-67 2000 mL in 1 PACKAGE; Type 0: Not a Combination Product 11/01/2018 07/31/2021 13 NDC:21749-713-65 192 mL in 1 PACKAGE; Type 0: Not a Combination Product 07/01/2021 14 NDC:21749-713-24 710 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 Drug 505G(a)(3) 11/01/2018 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-713) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 088312414 manufacture(21749-713) , label(21749-713) , pack(21749-713)