Otc - Active Ingredient
Allantoin 0.5%
Meijer Scar Gel
FDA Label NDC 79481-6285
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Meijer for the product Meijer Scar Gel (NDC 79481-6285). 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, dosage & administration, warnings, otc - keep out of reach of children, indications & usage, 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
Skin Protectant.
Dosage & Administration
Temporarily protects and helps relieve chapped or cracked skin.
Warnings
For external use only.
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if the condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days.
Do not use on deep or puncture wounds, animal bites, and serious burns.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If the product is swallowed, get medical help or contact a Poison Control Center right away.
Indications & Usage
Apply as needed.
Inactive Ingredient
Water, alcohol denat., PEG-4, glycerin, xanthan gum, allium cepa (onion) bulb extract, panthenol, sodium hyaluronate, aloe barbadensis leaf extract, chamomilla recutita (matricaria) flower extract, cucumis sativus (cucumber) fruit extract, tocopherol, juglans nigra (black walnut) leaf extract, benzyl alcohol, fragrance
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