Label: KINDEST KARE ADVANCED ANTIMICROBIAL HANDWASH- benzalkonium chloride liquid
- NDC Code(s): 11084-806-13, 11084-806-41
- 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 July 26, 2021
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
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Inactive ingredients
Aqua (Water), Hexylene Glycol, Cocamidopropylamine Oxide, PEG- 80 Sorbitan Laurate, Hydroxypropyl Methylcellulose, PEG-150 Distearate, PEG-8 Dimethicone, Sorbitol, Glycerin, Cocamidopropyl PG-Dimonium Chloride Phosphate, Cocamide MIPA, Soyamidopropylamine Oxide, Lauramine Oxide, Phenoxyethanol, Potassium Hydroxide, Citric Acid
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PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label
SCJ PROFESSIONAL
HEALTHCAREKindest Kare®
NDC 11084-806-41
Hand Soap
Antimicrobial Handwash
AdvancedHealth Personnel Handwash
Moisturising
Fragrance Free
Manufactured for:
SC Johnson Professional USA, Inc.
Charlotte, NC 28217
1-866-783-0422 www.scjp.com
Pat. www.scjp.com/patents
Made in Canada1 Liter SDS
(33.8 fl oz) (1.05 qt)REORDER #
6267-87deb
SKIN CARESAP # 4000000170
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INGREDIENTS AND APPEARANCE
KINDEST KARE ADVANCED ANTIMICROBIAL HANDWASH
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-806 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.7 mg in 100 mL Inactive Ingredients Ingredient Name Strength HEXYLENE GLYCOL (UNII: KEH0A3F75J) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) PEG-80 SORBITAN LAURATE (UNII: 239B50Y732) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) PEG-8 DIMETHICONE (UNII: GIA7T764OD) SORBITOL (UNII: 506T60A25R) GLYCERIN (UNII: PDC6A3C0OX) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11084-806-41 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/01/2018 2 NDC:11084-806-13 444 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/01/2018 06/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 02/01/2018 Labeler - SC Johnson Professional USA, Inc. (607378015) Establishment Name Address ID/FEI Business Operations STERIS Corporation 139424188 MANUFACTURE(11084-806) Establishment Name Address ID/FEI Business Operations APEX International, Inc. 015226132 MANUFACTURE(11084-806)