Otc - Active Ingredient
Ethyl Alcohol 62% w/w
The following Structured Product Label (SPL) was submitted to the FDA by The Clorox Company for the product Clorox Antimicrobial Hand Sanitizer (NDC 26509-0010). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - keep out of reach of children, dosage & administration, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Ethyl Alcohol 62% w/w
Antimicrobial
Uses
• To sanitize hands without requiring water or a rinse
Warnings
FLAMMABLE
For external use only
When using this product
• do not use near heat or flame
• do not use in or near eyes
• discontinue use if irritation and redness develop, or if condition persists for more than 72 hours
KEEP OUT OF REACH OF CHILDREN. In case of accidental ingestion, seek medical attention or contact a poison control center immediately.
Directions
• Wet hands thoroughly with product and allow to dry without wiping
Other Information
• Store at room temperature
Inactive ingredients
QUESTIONS OR COMMENTS?
Call 1-800-638-2625 or visit www.hlk.cc
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