Otc - Active Ingredient
Glycerin
Diona Cell Illuminating Booster
FDA Label NDC 72573-0002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Vaatz Co., Ltd. for the product Diona Cell Illuminating Booster (NDC 72573-0002). 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, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, 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
Inactive Ingredient
WATER, 1,2-HEXANEDIOL, NIACINAMIDE, SQUALANE, SODIUM DNA, ETC.
Otc - Purpose
Skin protectant
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
Apply an appropriate amount to skin and absorb it.
Warnings
1) If following symptoms occur after product use, stop using immediately and consult with a specialist: red spots, swelling, itchiness, and other skin irritations. 2) Avoid contact with eyes and open wounds. 3) Keep out of reach of children. 4) Do not store at high/low temperature. 5) Avoid direct sunlight.
Dosage & Administration
for external use only
Package Label.Principal Display Panel
1 (Label2)
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