Label: TORK HAND SANITIZER ALCOHOL FOAM- ethyl alcohol liquid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 49351-200-01 - Packager: ESSITY NORTH AMERICA 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 June 8, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
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PRINCIPAL DISPLAY PANEL
Tork Hand Sanitizer Alcohol Foam
Assainissant a base d'alcool pour les mains en mouse
TORK
Hand Sanitizer
Alcohol Foam
Ethyl alcohol 72%
Assainissant a Base
D'alcool
Pour les Mains en Mousse
Desinfectante de Manos
Espuma Con Alcohol
S4
40 02 16
Essity
Manufactured for / Fabrique pour / Fabricado para
Essity Professional Hygiene North America LLC
2929 Arch Street
Philadelphia, PA 19104
www.essity.com, www.torkusa.com
Patents/Brevets/Patentes: www.essity.com/patents
Manufactured for / Fabrique pour / Fabricado para
Essity Canada Inc.
1275 North Service Road W. Ste. 800
Oakville, ON L6M 3G4
www.tork.ca
Premium
950 mL
(32.1 US fl. oz.)
(33.4 oz. liq.)
NSF
FOR COMMERCIAL USE
POUR USAGE COMMERCIAL
PARA USO COMMERCIAL
MADE IN CANADA / FABRIQUE AUX
CANADA / HECHO EN CANADA
Peel here / Decoller ici / Despegar aqui -
INGREDIENTS AND APPEARANCE
TORK HAND SANITIZER ALCOHOL FOAM
ethyl alcohol liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49351-200 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.72 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYL ALCOHOL (UNII: 96F264O9SV) DIMETHICONE (UNII: 92RU3N3Y1O) BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T) DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1) PEG-200 DILAURATE (UNII: TWV5J70L88) GLYCERYL COCOATE (UNII: WVK1CT5994) COCO GLUCOSIDE (UNII: ICS790225B) GLYCERYL MONOOLEATE (UNII: C4YAD5F5G6) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49351-200-01 950 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/06/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 10/06/2014 Labeler - ESSITY NORTH AMERICA INC. (005694349) Registrant - SC Johnson Professional USA, Inc. (607378015) Establishment Name Address ID/FEI Business Operations SC Johnson Professional CA Inc. 203765300 manufacture(49351-200)