Otc - Purpose
Antibacterial
Wet Wipes Sanitizer
FDA Label NDC 77892-0004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Laber Kimya Ar-ge Sanayi Ticaret - Levent Kahriman for the product Wet Wipes Sanitizer (NDC 77892-0004). 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 - purpose, warnings, inactive ingredient, otc - active ingredient, indications & usage, otc - keep out of reach of children, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
For external use only.Keep out of the eyes. In case of eye contact, rinse with water.If irritation develps discontinue use and consult a doctor if irritation persists more than 72 hours. If swallowed, seek medical attention or contact a Poison Control Center.
Inactive Ingredient
Alcohol Denat (Ethanol) ,Glycerin, Melaleuca Alternifolia Leaf Extract, Hypericum Perforatum Extract, Chlorhexidine Gluconate , Aqua
Otc - Active Ingredient
% 80 Alcohol Denat (Ethanol)
Indications & Usage
ecreases bacteria on skin. recommended for repeated use
Otc - Keep Out Of Reach Of Children
Keep out of the reach of children, except with adult supervision.
Dosage & Administration
ake wipe and rub thoroughly over all surfaces of both hands.Rrub hands together briskly to dry·dispose of wipe. For children under 2 years ask a doctor before use.
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