Otc - Active Ingredient
niacinamide
Tania Pure Essence
FDA Label NDC 82237-0002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nfc Life Science Co.,ltd for the product Tania Pure Essence (NDC 82237-0002). 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
garlic fermented extract, etc.
Otc - Purpose
skin protectant
Otc - Keep Out Of Reach Of Children
Keep out of reach of the children
Indications & Usage
Take a proper amount after shower apply it gently according to skin texture, and wash it off to finish
Warnings
1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children
Dosage & Administration
for external use only
Package Label.Principal Display Panel
Label (Label)
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