Label: KINDEST KARE ANTIMICROBIAL FOAMING HANDWASH HEALTHCARE PERSONNEL HANDWASH- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 0519-1452-13, 0519-1452-41, 0519-1452-87, 0519-1452-91, view more0519-1452-92 - Packager: STERIS Corporation
- 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 3, 2014
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
- Use
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Warnings
For external use only
Discontinue use if irritation and redness develop. If irritation persists for more than 3 days, consult a physician.
- Directions
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Inactive ingredients
Water, Hexylene glycol, Propyl alcohol, Propylene glycol, Sorbitol, PEG-150 distearate, Sodium lauroyl methyl isethionate, PEG-45 palm kernel glycerides, PEG-7 glyceryl cocoate, C12-C15 alkyl benzoate, Ethanolamine lauroyl sarcosinate, Cocamide MEA, Diammonium EDTA, Citric acid, Ammonium lauryl sulfate, Ethanolamine, Fragrance
- Questions or comments?
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PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label
Kindest Kare®
Antimicrobial
Foaming HandwashNDC 0519-1452-41
Hand Soap
15
seconds
Fast-actingMild Fragrance
Antimicrobial
REORDER #
1452-FM1 Liter FSDS (33.8 fl oz) (1.05 qt)
STERIS®
STERIS Corporation ◾ 7501 Page Avenue ◾ St. Louis, MO 63133 ◾ USA
800-548-4873 ◾ www.steris.com1452-X7D(F)(1014)
62453
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INGREDIENTS AND APPEARANCE
KINDEST KARE ANTIMICROBIAL FOAMING HANDWASH HEALTHCARE PERSONNEL HANDWASH
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0519-1452 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan 0.75 g in 100 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) Hexylene glycol (UNII: KEH0A3F75J) Propyl alcohol (UNII: 96F264O9SV) Propylene glycol (UNII: 6DC9Q167V3) Sorbitol (UNII: 506T60A25R) PEG-150 distearate (UNII: 6F36Q0I0AC) sodium lauroyl methyl isethionate (UNII: II6VCD3S6R) Peg-45 Palm Kernel Glycerides (UNII: UC117W498W) PEG-7 glyceryl cocoate (UNII: VNX7251543) Alkyl (C12-15) benzoate (UNII: A9EJ3J61HQ) Lauroyl sarcosine (UNII: LIJ19P3L6F) Coco monoethanolamide (UNII: C80684146D) Edetic Acid (UNII: 9G34HU7RV0) Citric acid monohydrate (UNII: 2968PHW8QP) Ammonium lauryl sulfate (UNII: Q7AO2R1M0B) Monoethanolamine (UNII: 5KV86114PT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0519-1452-91 18 in 1 CASE 1 NDC:0519-1452-13 444 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:0519-1452-92 6 in 1 CASE 2 NDC:0519-1452-41 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:0519-1452-87 12 in 1 CASE 3 NDC:0519-1452-41 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 03/14/2006 Labeler - STERIS Corporation (139424188) Establishment Name Address ID/FEI Business Operations STERIS Corporation 139424188 MANUFACTURE(0519-1452)