Label: DEB INSTANTFOAM COMPLETE- alcohol liquid
- NDC Code(s): 11084-170-01, 11084-170-12, 11084-170-27, 11084-170-40
- 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
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
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PRINCIPAL DISPLAY PANEL
deb stoko
NDC 11084-170-27
Deb InstantFOAM Complete
EN Broad Spectrum Alcohol-Based Instant Hand Sanitizer Foam with Moisturizer and Skin Conditioner
Perfume-free Dye-free No water required Kills 99.999% of many types of common germs
ES Amplio espectro antiseptico con alcohol para manos en espuma y con acondicionador
Sin perfume Sin colorante No se requiere agua Elimina el 99.999% de los muchos tipos de germenes mas comunes
SANITIZE
deb
Stock #:
IFC1L
Made in / Hecho en Canada
US Patents 5,445,288 & 6,082,586
Worldwide Patent Pending.
Made by Deb for:
Deb USA, Inc.
Charlotte, NC 28217
1-800-248-7190
www.debgroup.com
DCN9207/0715
1 L
(33.8 fl oz)
Meets food code hand sanitizer criteria (Section 2-301.16) published by the FDA
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INGREDIENTS AND APPEARANCE
DEB INSTANTFOAM COMPLETE
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-170 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.80 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) COCO GLUCOSIDE (UNII: ICS790225B) DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1) GLYCERYL OLEATE (UNII: 4PC054V79P) PANTHENOL (UNII: WV9CM0O67Z) 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:11084-170-01 47 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/18/2015 2 NDC:11084-170-40 400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/18/2015 3 NDC:11084-170-27 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/18/2015 4 NDC:11084-170-12 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/18/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 08/18/2015 Labeler - SC Johnson Professional USA, Inc. (607378015) Registrant - SC Johnson Professional USA, Inc. (078805627) Establishment Name Address ID/FEI Business Operations SC Johnson Professional CA Inc. 203765300 manufacture(11084-170)