Label: TORK LIQUID ANTIBACTERIAL- chloroxylenol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 49351-201-01 - 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 December 14, 2018
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Ask a doctor before use if you have
- Stop use and ask a doctor
- Keep out of reach of children
- Directions
- Inactive ingredients
- Questions or Comments?
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PRINCIPAL DISPLAY PANEL
Tork Liquid Soap Antibacterial
Savon Liquide Antibacterien Tork
NDC 49351-201-01
TORK
Liquid Soap
Antibacterial
Chloroxylenol, 2.75%
Savon Liquide
Antibacterien
Jabon Liquido
Antibacteriano
S1
40 00 14
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
Premium
1L
(33.8 US fl. oz.)
(35.2 oz. liq.)
NSF
FOR COMMERCIAL USE
POUR USAGE COMMERCIAL
PARA USO COMMERCIAL
MADE IN USA / FABRIQUE AUX
ETATS-UNIS / HECHO EN EE. UU.
Peel here / Decoller ici / Despegar aqui
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INGREDIENTS AND APPEARANCE
TORK LIQUID ANTIBACTERIAL
chloroxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49351-201 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 2.75 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ETHYL ACRYLATE/METHACRYLIC ACID/STEARETH-20 METHACRYLATE COPOLYMER (UNII: EPA1872R1N) HEXYLENE GLYCOL (UNII: KEH0A3F75J) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49351-201-01 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/01/2015 Labeler - ESSITY NORTH AMERICA INC. (005694349) Registrant - Deb USA, Inc. (607378015) Establishment Name Address ID/FEI Business Operations Deb USA, Inc. 078805627 manufacture(49351-201)