Label: CLEAN CHOICE ALCOHOL SANITIZER- ethyl alcohol liquid
- NDC Code(s): 11084-704-12, 11084-704-27
- Packager: SC Johnson Professional USA, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 25, 2019
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- Active ingredient
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- Inactive ingredients
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PRINCIPAL DISPLAY PANEL
Clean Choice
NDC 11084-704-12
Foaming Alcohol Hand Sanitizer
UL ECOLOGO
PRODUCTS CERTIFIED FOR REDUCED ENVIRONMENTAL IMPACT. VIEW SPECIFIC ATTRIBUTES EVALUATED: UL.COM/EL
UL 2783
1 L (33.8 fl oz)
Stock # 0617388
DCN9254/0517
L-1417 R0
Distributed Exclusively by Fastenal
Distributed by Fastenal Company and its Subsidiaries
Winona, MN 55987
(C)2017 fastenal.com
Made in Canada
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INGREDIENTS AND APPEARANCE
CLEAN CHOICE ALCOHOL SANITIZER
ethyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-704 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 L in 100 L Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T) BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT) COCO GLUCOSIDE (UNII: ICS790225B) DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1) GLYCERYL OLEATE (UNII: 4PC054V79P) PEG-200 HYDROGENATED GLYCERYL PALMATE (UNII: W161T051Y1) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11084-704-27 1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/15/2013 2 NDC:11084-704-12 1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/28/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 09/15/2013 Labeler - SC Johnson Professional USA, Inc. (607378015) Establishment Name Address ID/FEI Business Operations SC Johnson Professional CA Inc. 203765300 manufacture(11084-704)