Eezysun Aloe Vera After Sun
FDA Label NDC 70116-011
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bio Earth Manufacturing (pty) Ltd for the product Eezysun Aloe Vera After Sun (NDC 70116-011). 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 ingredients, purpose, uses, warnings, directions, inactive ingredients, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Aniba Rosaedora 0.1%, Calendula Officinails 0.1% , Hyaluronic Acid 0.5%, Lavandula Officinalis 0.3%, Matricaria Chamomilla 0.4%, Mentha Piperita 0.15%
Purpose
Relaxing, cooling, anti-inflammatory, soothing, relieving
Uses
Cooling down and healing the skin. Alleviating the pain and swelling a
associated with over-exposure to the sun.
Warnings
Not suitable for epileptics, Not suitable for people with uncontrolled
hyper-tension. Not recommended during pregnancy and lactation,
Not suitable for individuals with known sensitivity to any of the
ingredients. For external use only. Avoid contact with eyes.
Directions
Adults: Apply up to three times per day as needed
Children: Use conservatively for children younger than two years
Inactive Ingredients
Carbomer, Glycerin, Methylparaben, Methyl Sulfonyl Methane (MSM), Propylparaben, Triethanolamine, Water
Product Label
Image Description (Image 5 V1)
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