Otc - Active Ingredient
Sodium Hyaluronate 0.005%
Miracle Aqua Peeling
FDA Label NDC 72557-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Toas Co., Ltd. for the product Miracle Aqua Peeling (NDC 72557-001). 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 - active ingredient, otc - purpose, indications & usage, dosage & administration, warnings, otc - keep out of reach of children, inactive ingredient, 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
Otc - Purpose
Moisturizing
Indications & Usage
Helps to keep skin moistness
Dosage & Administration
Apply a generous amount on face and gently massage.
Rinse thoroughly.
Warnings
For external use only.
Do not use on damaged or broken skin.
When using this product, keep out of eyes. Rinse with water to remove.
Stop using and ask a doctor if rash occurs.
Otc - Keep Out Of Reach Of Children
Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.
Inactive Ingredient
Water, 1,2-Hexanediol, Alcohol, Arginine, Butylene Glycol, Camellia Sinensis Leaf Extract, Canavalia Gladiata Seed Extract, Carbomer, Caviar Extract, Cellulose, Centella Asiatica Extract, Chamomilla Recutita (Matricaria) Flower Extract, Ethylhexylglycerin, Fragrance, Glycyrrhiza Glabra (Licorice) Root Extract, Nasturtium Offcinale Extract, PEG-400, PEG-60 Hydrogenated Castor Oil , Polygonum Cuspidatum Root Extract, Rosmarinus Officinalis (Rosemary) Leaf Exreact, Scutellaria Baicalensis Root Extract, Tocopheryl Acetate
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