FDA Label for Exp Foaming Hand Sanitizer
View Indications, Usage & Precautions
Exp Foaming Hand Sanitizer Product Label
The following document was submitted to the FDA by the labeler of this product Kay Chemical Company. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Benzalkonium chloride 0.1%
Purpose
Antiseptic handwash
Uses
- for handwashing to decrease bacteria on the skin
Warnings
For external use only
Do Not Use
- in eyes
Otc - When Using
- if in eyes, rinse promptly and thoroughly with water
- discontinue use if irritation and redness develop
Otc - Ask Doctor
Stop use and ask a doctor if skin irritation or redness occurs for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Direction
- wet hands thoroughly with product and allow to dry without wiping.
- do not use if hands are visibly dirty or greasy; wash hands with soap and water instead.
Other Information
- for additional information, see Safety Data Sheet (SDS)
- EMERGENCY HEALTH INFORMATION: 1 877 231 2615. If located outside the United States and Canada, call collect 952 853 1713 (number is in the US).
Inactive Ingredient
Inactive ingredients water (aqua), isopropyl alcohol, propylene glycol, FD&C red 40, FD&C blue 1
Otc - Questions
Questions? call 1-800-529-5458
Principal Display Panel And Representative Label
ECOLAB
NDC 63146-320-16
EXP Foaming
Hand Sanitizer
Active Ingredient: Benzalkonium chloride 0.1%
1200 mL
(40.6 US FL OZ) 1112848
Kay Chemical Company · 8300 Capital Drive
Greensboro, NC 27409-9790 USA
Customer Service: (800) 529-5458
©2024 Kay Chemical Company
All rights reserved
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782982/8000/0224
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