Instant Hand Sanitizer
FDA Label NDC 42302-030
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lonkey Overseas Inc. for the product Instant Hand Sanitizer (NDC 42302-030). 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 drug facts, active ingredient:, purpose, uses:, warnings, other safety information, otc - do not use, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient:
Ethyl Alcohol 62% w/w
Purpose
Antiseptic
Uses:
For handwashing to decrease bacteria on the skin.
Recommended for repeated use.
Warnings
For external use only.
Other Safety Information
Flammable, keep away from fire or flame.
Otc - Do Not Use
Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develop and persist 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.
Directions
Wet hands thoroughly with product. Briskly rub hands together until dry.
Supervise children in the use of this product.
Inactive Ingredients
Ethanol, Deionized water, Carbomer, Triethanolamine, 2H-1-Benzopyran-6-ol,3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-acetate.
Other Information
Do not store above 105 degrees F.
May discolor some fabrics or surfaces.
This product is not made by "PFIZER Industries Inc."
Owner of the registered trademark "Purell"
All Rights Reserved
Distributed By:
LONKEY OVERSEAS INCORPORATION
MADE IN CHINA
Instant Hand Sanitizer 8Oz/236Ml (42302-030-00)
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