Otc - Active Ingredient
Niacinamide
Diapia Ha Aqua Shining Mask
FDA Label NDC 71857-0013
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bsg H & B Co., Ltd. for the product Diapia Ha Aqua Shining Mask (NDC 71857-0013). 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, Butylene Glycol, Glycereth-26, Glycerin, Methylpropanediol, 1,2-Hexanediol, Phenoxyethanol, Carbomer, Hydroxyethyl Urea, Triethanolamine, Dipotassium Glycyrrhizate, Allantoin, PEG/PPG-17/6 Copolymer, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Saccharide Isomerate, Xanthan Gum, Tetrasodium EDTA, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Sodium Hyaluronate, Vaccinium Angustifolium (Blueberry) Fruit Extract,
Rubus Idaeus (Raspberry) Fruit Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Euterpe Oleracea Fruit Extract, Fragaria Chiloensis (Strawberry) Fruit Extract, Fragrance, Sodium Citrate, Citric Acid, Polyglutamic Acid, Hydroxyethylcellulose
Otc - Purpose
Brightening, Moisturizing, Softening, Soothing
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
Cleanse and dry face thoroughly.
Open pouch, unfold mask and apply to face.
Leave it for 10 - 20 minutes, remove the mask and tap slightly until essence
absorbed.
Warnings
1.Keep out of reach of children.
2.Store in a cool, dry place and avoid direct sunlight.
3.If abnormal symptoms occur after use, stop use and consult with a skin specialist.
Dosage & Administration
for external use only
Package Label.Principal Display Panel
Label (Label)
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