Active Ingredient
Ethyl Alcohol 75%V/V
Hand Sanitizer
FDA Label NDC 52807-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Longtai Industry Co.,ltd for the product Hand Sanitizer (NDC 52807-101). 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 active ingredient, purpose, uses, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Purpose: Antimicrobial
Uses
For hand washing to decrease bacteria on the skinre commended for repeated use
Warnings
KEEP AWAY FROM FLAMDo not use in the eyes. In case of contact, rinse eyeswith wafer
Do Not Use
- Do not use in the eyes. In case of contact, rinse eye soughly with wafer
Otc - When Using
/
Otc - Stop Use
Stop use and ask a doctor f irriration and renews 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 hans together until dry Supervise children under 6 years old in the use of this product.
Other Information
- Store at 20 to 25C(68 to 77 F)
Inactive Ingredients
water, Glycerin, CaromAloe vera, Aminomethyl propanol Vitamin E
Package Label - Principal Display Panel
1 (106 250)
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