Active Ingredient(S)
Ethyl Alcohol 80%
Lactone Hand Sanitizer Wipe
FDA Label NDC 75348-888
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by All One Kozmetik Sanayi Dis Ticaret Anonim Sirketi for the product Lactone Hand Sanitizer Wipe (NDC 75348-888). 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(s), purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Use for hand-washing to decrease bacteria on the skin, only when water is not available
Warnings
Flammable, keep away from heat and flames. For external use only
Otc - When Using
When using this product
do not get into eyes
if contact occurs, rinse eyes thoroughly with water
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs.
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 thorougly with product and allow to dry without wiping
Inactive Ingredients
water, Aloe Barbadensis Leaf Extract and propylene glycol
Package Label - Principal Display Panel
Producer
ALL ONE KOZMETIK SAN. VE DIS. TIC. A. S.
Sutluce Mahallesi
Uzunbayır Sokak No:44/4
Beyoglu/Istanbul
Net weight: 5 gr
MADE IN TURKEY
Hand Sanitizer Wipe
Kills 99.99% of E. coli, Salmonella enterica and Staphylococcus aureus (MRSA)
with ALOE VERA FRAGRANCE
For External Use only
LACTONE HAND SANITIZING WIPES- alcohol cloth
Puch (A74550d3 Faef 0f2b E053 2995a90a6b2a)
Package (Download)
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