Label: DEB INSTANTFOAM ALCOHOL SANITIZER- ethyl alcohol liquid
- NDC Code(s): 11084-703-02, 11084-703-12, 11084-703-27, 11084-703-40
- 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 26, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
-
PRINCIPAL DISPLAY PANEL
NDC 11084-703-27
deb stoko
Deb InstantFOAM
Alcohol Hand Sanitizer
No Water Required | Kills 99.999% of Common GermsAntiséptico para manos en espuma - con alcohol
No se requiere agua | Elimina el 99.999% de los gérmenes más
comunesSANITIZE
1 L (33.8 FL OZ)
Stock #IFS1L
Deb USA, Inc., 1-800-248-7190, www.debgroup.com
Made in Canada, DCN9313 L-1251 R6
OPEN FOR DRUG FACTS
-
INGREDIENTS AND APPEARANCE
DEB INSTANTFOAM ALCOHOL SANITIZER
ethyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-703 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) DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1) BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T) DIMETHICONE (UNII: 92RU3N3Y1O) COCO GLUCOSIDE (UNII: ICS790225B) PEG-200 DILAURATE (UNII: TWV5J70L88) GLYCERYL COCOATE (UNII: WVK1CT5994) GLYCERYL MONOOLEATE (UNII: C4YAD5F5G6) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11084-703-27 1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/15/2012 2 NDC:11084-703-12 1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/15/2012 3 NDC:11084-703-40 .4 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/15/2012 4 NDC:11084-703-02 .047 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/15/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/15/2012 Labeler - SC Johnson Professional USA, Inc. (607378015) Establishment Name Address ID/FEI Business Operations SC Johnson Professional CA Inc. 203765300 manufacture(11084-703)