Label: KINDEST KARE ADVANCED ANTIMICROBIAL FOAM HANDWASH- benzalkonium chloride liquid
-
NDC Code(s):
11084-807-12,
11084-807-13,
11084-807-27,
11084-807-41, view more11084-807-66
- 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 March 1, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Uses
- Warnings
- Directions
-
Inactive ingredients
Aqua (Water), Hexylene Glycol, Glycerin, PEG-8 Dimethicone, PEG-150 Distearate, Sorbitol, Decyl Glucoside, Soyamidopropyl Amine Oxide, Cocamide MIPA, Cetyl Hydroxyethylcellulose, Polyquaternium-7, Cocamidopropyl PG-Dimonium Chloride Phosphate, Cocamidopropyl Amine Oxide, Lauramine Oxide, Citric Acid, Potassium Hydroxide, Phenoxyethanol.
- Questions or comments?
-
PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label
SCJ PROFESSIONAL
HEALTHCAREKindest Kare®
NDC 11084-807-27
Hand Soap
Antimicrobial Foam Soap AdvancedHealth Personnel Handwash
Moisturizing
Fragrance FreeManufactured for :
SC Johnson Professional USA, Inc.
Charlotte, NC 28217
1-866-783-0422
www.scjp.com
Pat. www.scjp.com/patents
Made in USA1 Liter (33.8 fl oz)
(1.05 qt)SAP # 4000000171
REORDER #
626461deb
SKIN CAREOpen for
Drug Facts -
INGREDIENTS AND APPEARANCE
KINDEST KARE ADVANCED ANTIMICROBIAL FOAM HANDWASH
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-807 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.5 mg in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) HEXYLENE GLYCOL (UNII: KEH0A3F75J) GLYCERIN (UNII: PDC6A3C0OX) PEG-8 DIMETHICONE (UNII: GIA7T764OD) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) SORBITOL (UNII: 506T60A25R) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1) CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11084-807-41 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/01/2018 2 NDC:11084-807-13 444 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/01/2018 3 NDC:11084-807-27 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/01/2018 4 NDC:11084-807-12 1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/01/2018 5 NDC:11084-807-66 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/17/2023 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 APEX International, Inc. 015226132 MANUFACTURE(11084-807)